| Diseases |
Alias |
|
| Mccune-Albright Syndrome |
|
Mass Syndrome
|
Polyostotic Fibrous Dysplasia
|
|
MAS
|
Fibrous Dysplasia Of Bone
|
|
Albright Syndrome
|
Mass Phenotype
|
|
Overlap Connective Tissue Disease
|
Mccune Albright Syndrome
|
|
Osteitis Fibrosa Disseminata
|
OCTD
|
|
Albright'S Disease
|
Pfd
|
|
Pofd
|
Albright'S Syndrome
|
|
Mccune-Albright Syndrome, Somatic, Mosaic
|
Albright'S Disease Of Bone
|
|
Albright'S Syndrome With Precocious Puberty
|
Albright-Mccune-Sternberg Syndrome
|
|
Albright-Sternberg Syndrome
|
Fibrous Dysplasia With Pigmentary Skin Changes And Precocious Puberty
|
|
Gonadotropin-Independent Female-Limited Sexual Precocity
|
Fibrous Dysplasia Polyostotic
|
|
Fibrous Dysplasia, Polyostotic
|
|
|
| Pseudohypoparathyroidism, Type Ia |
|
Albright'S Hereditary Osteodystrophy
|
Albright Hereditary Osteodystrophy
|
|
Pseudohypoparathyroidism Type 1a
|
PHP1A
|
|
Albright Hereditary Osteodystrophy With Multiple Hormone Resistance
|
Pseudohypoparathyroidism Ia
|
|
AHO
|
Pseudohypoparathyroidism With Albright Hereditary Osteodystrophy
|
|
Pseudo-Pseudohypoparathyroidism
|
Pseudohypoparathyroidism Type I A
|
|
Php Ia
|
Pseudopseudohypoparathyroidism
|
|
Albright Hereditary Osteodystrophy Without Multiple Hormone Resistance
|
Pphp
|
|
Pseudopseudo-Hypoparathyroidism
|
Aho-Php Syndrome Ia
|
|
Albright Hereditary Osteodystrophy-Php Syndrome Ia
|
Pseudohypoparathyroidism 1a
|
|
Pseudohypoparathyroidism
|
|
|
| Osseous Heteroplasia, Progressive |
|
Progressive Osseous Heteroplasia
|
POH
|
|
Osteoma Cutis
|
Familial Ectopic Ossification
|
|
Ectopic Ossification Familial Type
|
Ectopic Ossification
|
|
Heterotopic Ossification
|
Ectopic Ossification, Familial
|
|
Cutaneous Ossification
|
Myositis Ossificans Progressiva
|
|
Osteodermia
|
Osteosis Cutis
|
|
Ossification Heterotopic
|
Heteroplasia, Osseous, Progressive
|
|
Fibrodysplasia Ossificans Progressiva
|
|
|
| Pseudohypoparathyroidism, Type Ic |
|
Pseudohypoparathyroidism Type 1c
|
PHP1C
|
|
Pseudohypoparathyroidism Ic
|
Php Ic
|
|
Pseudohypoparathyroidism 1c
|
|
|
| Pseudohypoparathyroidism, Type Ib |
|
Pseudohypoparathyroidism Type 1b
|
PHP1B
|
|
Pseudohypoparathyroidism Ib
|
Pseudohypoparathyroidism Type Ib
|
|
Php Ib
|
Pseudohypoparathyroidism 1b
|
|
|
| Pseudopseudohypoparathyroidism |
|
PPHP
|
Albright Hereditary Osteodystrophy Without Multiple Hormone Resistance
|
|
Normocalcemic Pseudohypoparathyroidism
|
Aho-Pphp Syndrome
|
|
Albright Hereditary Osteodystrophy-Pphp Syndrome
|
Pseudohypoparathyroidism
|
|
|
| Acth-Independent Macronodular Adrenal Hyperplasia |
|
Acth-Independent Macronodular Adrenocortical Hyperplasia
|
Adrenocorticotropic Hormone-Independent Macronodular Adrenal Hyperplasia
|
|
Corticotropin-Independent Macronodular Adrenal Hyperplasia
|
Cushing Syndrome Due To Macronodular Adrenal Hyperplasia
|
|
AIMAH1
|
Aimah
|
|
Massive Macronodular Adrenocortical Disease
|
Mmad
|
|
Primary Macronodular Adrenal Hyperplasia
|
Cushing Syndrome, Adrenal, Due To Aimah
|
|
Primary Bilateral Macronodular Adrenal Hyperplasia
|
Acth-Independent Macronodular Adrenal Hyperplasia 1
|
|
Acth-Independent Cushing Syndrome
|
Adrenal Cushing Syndrome Due To Aimah
|
|
Acth-Independent Macronodular Adrenal Hyperplasia 2
|
|
|
| Pituitary Adenoma 3, Multiple Types |
|
PITA3
|
Pituitary Adenoma 3, Multiple Types, Somatic
|
|
Pituitary Adenoma 3
|
|
|
| Pseudohypoparathyroidism |
|
Familial Pseudohypoparathyroidism
|
Parathyroid Hormone Resistant Hypoparathyroidism
|
|
Php - [Pseudohypoparathyroidism]
|
Constitutional Chronic Hypocalcaemia
|
|
|
| Brachydactyly |
|
|
| Monostotic Fibrous Dysplasia |
|
Jaffe-Lichtenstein Disease
|
Fibrous Dysplasia Monostotic
|
|
Fibrous Dysplasia, Monostotic
|
|
|
| Spastic Paraplegia 4, Autosomal Dominant |
|
SPG4
|
Hereditary Spastic Paraplegia 4
|
|
Fsp2
|
Autosomal Dominant Spastic Paraplegia Type 4
|
|
Familial Spastic Paraplegia, Autosomal Dominant, 2
|
Autosomal Dominant Spastic Paraplegia 4
|
|
Familial Spastic Paraplegia Autosomal Dominant 2
|
Paraplegia, Spastic, Autosomal Dominant, Type 4
|
|
|
| Conn'S Syndrome |
|
Cushing Syndrome
|
Hyperaldosteronism
|
|
Primary Hyperaldosteronism
|
Hypercortisolism
|
|
Primary Aldosteronism
|
Cushing'S Syndrome
|
|
Adrenal Gland Hyperfunction
|
Conn Syndrome
|
|
Hyperadrenalism
|
Ectopic Acth Syndrome
|
|
Hyperadrenocorticism
|
Cushing Disease
|
|
Cushing'S Disease
|
Adrenal Cortex Adenoma
|
|
Corticotroph Pituitary Adenoma
|
Pituitary Corticotroph Micro-Adenoma
|
|
Pituitary-Dependent Cushing Syndrome
|
Pituitary Acth Hypersecretion
|
|
Acth Syndrome, Ectopic
|
Acth-Secreting Pituitary Adenoma
|
|
Adrenal Hyperfunction Resulting From Pituitary Acth Excess
|
Ectopic Adrenocorticotropic Hormone Syndrome
|
|
Nodular Primary Adrenocortical Dysplasia
|
Pituitary Dependent Cushing Syndrome
|
|
Pituitary Cushing Syndrome
|
Pituitary-Dependant Cushing Syndrome
|
|
Pituitary-Dependant Hypercortisolism
|
Pituitary-Dependant Hypercortisolism Disorder
|
|
Aldosteronism Primary
|
Acth Syndrome Ectopic
|
|
Adrenal Cushing'S Syndrome
|
Adrenal Cortical Adenoma
|
|
Cushing Syndrome Nos
|
Cortisol Hypersecretion
|
|
Corticoadrenal Hypersecretion
|
Cushing Syndrome Secondary To Ectopic Acth-Secretion
|
|
Ectopic Cushing Syndrome
|
Hypercortisolism Due To Nonpituitary Tumour
|
|
Ectopic Acth - [Adrenocorticotropic Hormone] Secretion
|
Ectopic Acth - [Adrenocorticotropic Hormone] Secretion Causing Cushing Syndrome
|
|
Idiopathic Aldosteronism
|
Aldosteronism
|
|
Primary Aldosteronism Due To Bilateral Adrenal Hyperplasia
|
Primary Aldosteronism Due To Adrenal Hyperplasia
|
|
|
| Body Mass Index Quantitative Trait Locus 11 |
|
OBESITY
|
Obesity, Susceptibility To
|
|
Leanness, Inherited
|
Obesity, Susceptibility To, Bmiq11
|
|
Obesity, Mild, Early-Onset
|
Obesity, Association With
|
|
Obesity, Early-Onset, Susceptibility To
|
Obesity, Severe
|
|
Obesity, Severe, And Type Ii Diabetes
|
Obesity, Late-Onset
|
|
Obesity , Susceptibility To
|
BMIQ11
|
|
Obesity Bmiq11
|
Obesity, Early-Onset
|
|
Simple Obesity Nos
|
Excess Fat
|
|
Obesity, Not Elsewhere Classified, Body Mass Index Not Elsewhere Classified
|
Adiposis
|
|
|
| Acth-Independent Macronodular Adrenal Hyperplasia 1 |
|
Aimah1
|
Hyperplasia, Adrenal, Acth-Independent, Macronodular, Type 1
|
|
|
| Fibrous Dysplasia / Mccune-Albright Syndrome |
|
Fibrous Dysplasia/Mccune-Albright Syndrome
|
Fd/Mas
|
|
Fd/Mas Spectrum
|
Fd/Mas Syndrome
|
|
Fibrous Dysplasia/Mccune-Albright Spectrum
|
|
|
| Fibrous Dysplasia |
|
Fibrous Dysplasia Of Bone
|
|
|
| Pituitary Tumors |
|
Pituitary Tumor
|
Pituitary Neoplasms
|
|
|
| Mazabraud Syndrome |
|
Myxoma With Fibrous Dysplasia
|
Fibrous Dysplasia Of Bone With Intramuscular Myxoma
|
|
|
| Acth-Independent Cushing Syndrome |
|
Adrenal Cushing Syndrome
|
Adrenocorticotropic Hormone-Independent Cushing Syndrome
|
|
Corticotropin-Independent Cushing Syndrome
|
|
|
| Hyperthyroidism |
|
|
| Pancreatic Adenocarcinoma |
|
Adenocarcinoma Of The Pancreas
|
Adenocarcinoma Of Pancreas
|
|
Pancreas Adenocarcinoma
|
Malignant Exocrine Neoplasm
|
|
Primary Pancreatic Adenocarcinoma
|
Adenocarcinoma Of Islet Cell Of Pancreas
|
|
Islet Cell Adenocarcinoma Of Unspecified Site
|
Mixed Adenocarcinoma Islet Cell With Exocrine Of Unspecified Site
|
|
|
| Adenoma |
|
Acinar Cell Adenoma
|
Adenomas
|
|
Acinic Cell Adenoma
|
|
|
| Acromegaly |
|
Gigantism
|
Growth Hormone Excess
|
|
Pituitary Giant
|
Somatotroph Adenoma
|
|
Growth Hormone-Secreting Pituitary Adenoma
|
|
|
| Precocious Puberty |
|
Familial Precocious Puberty
|
Idiopathic Sexual Precocity
|
|
Sexual Precocity
|
Puberty Precocious
|
|
Cryptogenic Sexual Precocity
|
|
|
| Hypothyroidism, Congenital, Nongoitrous, 1 |
|
Tsh Resistance
|
CHNG1
|
|
Hypothyroidism Due To Tsh Receptor Mutations
|
Thyrotropin Resistance
|
|
Thyroid-Stimulating Hormone
|
Rtsh
|
|
Hypothyroidism Due To Unresponsiveness To Thyrotropin
|
Congenital Nongoitrous Hypothyroidism 1
|
|
Thyroid-Stimulating Hormone, Resistance To
|
Hypothyroidism, Nonautoimmune
|
|
Hypothyroidism, Congenital, Due To Tsh Resistance
|
Hypothyroidism, Congenital, Non-Goitrous, 1
|
|
Congenital Hypothyroidism Due To Tsh Resistance
|
Non-Autoimmune Hypothyroidism
|
|
Thyroid-Stimulating Hormone Resistance
|
Hypothyroidism, Congenital, Nongoitrous, Type 1
|
|
Hypothyroidism, Congenital, Nongoitrous, 3
|
Thyroid Hormone Resistance Syndrome
|
|
|
| Hyperphosphatemia |
|
|
| Adrenal Cortical Carcinoma |
|
Adrenocortical Carcinoma
|
Adrenal Cortex Carcinoma
|
|
Carcinoma Of The Adrenal Cortex
|
Acc
|
|
Adrenocortical Cancer
|
Carcinoma Adrenocortical
|
|
|
| Multinodular Goiter |
|
|
| Graves' Disease |
|
Graves Disease
|
Exophthalmic Goiter
|
|
Basedow'S Disease
|
Grave'S Disease
|
|
Basedow Disease
|
Toxic Diffuse Goiter
|
|
Graves' Hyperthyroidism
|
Parry Disease
|
|
Autoimmune Hyperthyroidism
|
Toxic Multinodular Goiter
|
|
|
| Growth Hormone Secreting Pituitary Adenoma |
|
Somatotroph Adenoma
|
Growth Hormone-Secreting Pituitary Adenoma
|
|
Growth Hormone Producing Adenoma Of The Pituitary
|
Growth Hormone Secreting Adenoma Of Pituitary
|
|
|
| Pseudomyxoma Peritonei |
|
Adenomucinosis
|
Gelatinous Ascites
|
|
Pmp
|
Mucinous Ascites
|
|
Syndrome Of Pseudomyxoma Peritonei
|
|
|
| Appendiceal Neoplasm |
|
Appendix Neoplasm
|
Neoplasm Of Appendix
|
|
Appendiceal Neoplasms
|
Appendiceal Cancer
|
|
Appendix Cancer
|
Malignant Neoplasm Of Appendix Vermiformis
|
|
Malignant Tumour Of Appendix
|
|
|
| Osteitis Fibrosa |
|
Osteitis Fibrosa Cystica
|
Hyperparathyroid Bone Disease
|
|
Osteitis Fibrosa Cystica Generalisata
|
Von Recklinghausen'S Bone Disease
|
|
Osteitis Fibrosa Disseminata
|
|
|
| Cholera |
|
Vibrio Cholerae Infection
|
Cholera - Vibrio Cholerae
|
|
Cholera Due To Vibrio Cholerae
|
Vibrio Cholerae
|
|
Cholera Syndrome
|
Asiatic Cholera
|
|
Epidemic Cholera
|
|
|
| Gastric Adenocarcinoma |
|
Adenocarcinoma Of Stomach
|
Stomach Adenocarcinoma
|
|
Adenocarcinoma Gastric
|
Intestinal Type Adenocarcinoma Of Unspecified Site
|
|
Diffuse Type Adenocarcinoma Of Unspecified Site
|
|
|
| Skin Melanoma |
|
Cutaneous Melanoma
|
Malignant Ear Melanoma
|
|
Malignant Lip Melanoma
|
Malignant Lower Limb Melanoma
|
|
Malignant Melanoma Of Ear And/Or External Auricular Canal
|
Malignant Melanoma Of Skin Of Lower Limb
|
|
Malignant Melanoma Of Skin Of Trunk Except Scrotum
|
Malignant Melanoma Of Skin Of Upper Limb
|
|
Malignant Neck Melanoma
|
Malignant Scalp Melanoma
|
|
Malignant Trunk Melanoma
|
Malignant Upper Limb Melanoma
|
|
Melanoma, Cutaneous Malignant
|
Melanoma
|
|
Malignant Melanoma Of Skin
|
Melanoma Nos
|
|
Malignant Mole, Meaning Melanoma Of Unspecified Site
|
Melanoma Of Unspecified Site
|
|
Cutaneous Malignant Melanoma
|
Mm - [Malignant Melanoma]
|
|
|
| Goiter |
|
|
| Congenital Hypothyroidism |
|
Cretinism
|
Neonatal Hypothyroidism
|
|
Ch
|
Cht
|
|
Congenital Myxedema
|
Myxedema, Congenital
|
|
Endemic Cretinism
|
Congenital Iodine-Deficiency Syndrome
|
|
Fetal Iodine Deficiency Syndrome
|
Congenital Iodine-Deficiency Hypothyroidism Nos
|
|
|
| Endocrine Gland Cancer |
|
Endocrine Neoplasm
|
Malignant Neoplasm Of Endocrine Gland
|
|
Endocrine Gland Neoplasms
|
Endocrine Tumor
|
|
Malignant Endocrine Tumor
|
Malignant Tumour Of Endocrine Gland
|
|
Neoplasm Of Endocrine Gland
|
Neoplasm Of Endocrine System
|
|
Neoplasm Of The Endocrine System
|
Carcinoma Of Endocrine Gland
|
|
|
| Hyperprolactinemia |
|
Chiari-Frommel Syndrome
|
Hyperprolactinaemia
|
|
Familial Hyperprolactinemia
|
HPRL
|
|
Pregnancy-Related A-G Syndrome
|
Familial Isolated Prolactin Receptor Deficiency
|
|
|
| Pituitary Adenoma |
|
Adenoma Of The Pituitary Gland
|
Pituitary Adenomas
|
|
Adenoma, Pituitary
|
Pituitary Gland Adenoma
|
|
Pituitary Neoplasms
|
|
|
| Multiple Endocrine Neoplasia |
|
Men
|
Multiple Endocrine Adenomatosis
|
|
Multiple Endocrine Neoplasia Syndrome
|
Adenomatosis, Familial Endocrine
|
|
Endocrine Neoplasia, Multiple
|
Familial Endocrine Adenomatosis
|
|
Mea
|
Multiple Endocrine Neoplasms
|
|
Multiple Endocrine Neoplasia Type 1
|
|
|
| Appendix Disease |
|
|
| Appendix Cancer |
|
Appendiceal Neoplasms
|
Cancer Of The Appendix
|
|
Malignant Neoplasm Of Appendix Vermiformis
|
Malignant Tumor Of Appendix
|
|
Malignant Tumor Of The Appendix
|
Malignant Neoplasm Of Appendix
|
|
Carcinoma Of The Appendix
|
|
|
| Acrodysostosis |
|
Acrodysplasia
|
Arkless-Graham Syndrome
|
|
Maroteaux-Malamut Syndrome
|
Nasal Hypoplasia-Peripheral Dysostosis-Intellectual Disability Syndrome
|
|
Peripheral Dysostosis-Nasal Hypoplasia-Intellectual Disability Syndrome
|
|
|
| Multiple Endocrine Neoplasia, Type I |
|
Multiple Endocrine Neoplasia Type 1
|
MEN1
|
|
Wermer Syndrome
|
Multiple Endocrine Neoplasia 1
|
|
Multiple Endocrine Neoplasia, Type 1
|
Men I
|
|
Endocrine Adenomatosis, Multiple
|
Mea I
|
|
Men Type I
|
Wermer'S Syndrome
|
|
Men1 Syndrome
|
Multiple Endocrine Adenomatosis
|
|
Endocrine Adenomatosis Multiple
|
Men 1
|
|
Familial Multiple Endocrine Neoplasia Type I
|
Neoplasia, Endocrine, Multiple, Type 1
|
|
Multiple Endocrine Neoplasia
|
|
|
| Osteofibrous Dysplasia |
|
Ofd
|
OSFD
|
|
Jaffe-Campanacci Syndrome
|
Ossifying Fibroma
|
|
Osteofibrous Dysplasia, Susceptibility To
|
Tibia, Bowing Of, With Pseudarthrosis And Pectus Excavatum
|
|
Intracortical Fibrous Dysplasia
|
Bowing Of Tibia With Pseudarthrosis And Pectus Excavatum
|
|
Dysplasia, Osteofibrous, Susceptibility To
|
|
|
| Ovarian Cyst |
|
|
| Ossifying Fibroma |
|
Peripheral Ossifying Fibroma
|
Fibro-Osteoma
|
|
Fibroma Ossifying
|
Fibroma, Ossifying
|
|
|
| Cervical Cancer |
|
Cervical Cancer, Somatic
|
Neoplasm Of Uterine Cervix
|
|
Cervix Cancer
|
Uterine Cervical Neoplasm
|
|
Cervical Neoplasm
|
Cervix Uteri Cancer
|
|
Tumor Of The Cervix Uteri
|
CERCA
|
|
Uterine Cervical Cancer
|
Neoplasms Cervical
|
|
Uterine Cervical Neoplasms
|
Cervical Cancers
|
|
Cancer, Cervical, Somatic
|
Malignant Tumor Of Cervix
|
|
Cervix Carcinoma
|
|
|
| Peutz-Jeghers Syndrome |
|
PJS
|
Polyposis, Hamartomatous Intestinal
|
|
Polyps-And-Spots Syndrome
|
Lentiginosis, Perioral
|
|
Periorificial Lentiginosis Syndrome
|
Hamartomatous Intestinal Polyposis
|
|
Hamartomatous Polyp
|
Colonic Hamartomatous Polyp
|
|
Gastric Peutz-Jeghers Polyp
|
Peutz Jeghers Colon Polyp
|
|
Peutz Jeghers Polyp
|
Peutz-Jeghers Polyp Of Small Intestine
|
|
Peutz-Jeghers Small Bowel Hamartoma
|
Peutz Jeghers Polyposis
|
|
Intestinal Polyposis-Cutaneous Pigmentation Syndrome
|
Peutz-Jeghers Polyposis
|
|
Polyposis, Intestinal, Ii
|
Intestinal Hamartomatous Polyposis
|
|
Peutz-Jeghers Polyp
|
Peutz-Jeghers Polyp Of The Stomach
|
|
Peutz Jehgers Polyp
|
Peutz-Jeghers Polyps Of Small Bowel
|
|
|
| Mulchandani-Bhoj-Conlin Syndrome |
|
MBCS
|
Maternal Uniparental Disomy Of Chromosome 20
|
|
Maternal Upd(20)
|
Upd(20)Mat
|
|
Uniparental Disomy, Maternal, Chromosome 20
|
|
|
| Peripheral Osteosarcoma |
|
Surface Osteosarcoma
|
Bone Surface Osteosarcoma
|
|
|
| Lung Cancer Susceptibility 3 |
|
Lung Adenocarcinoma
|
Adenocarcinoma Of Lung
|
|
LNCR3
|
Adenocarcinoma Of Lung, Susceptibility To
|
|
Bronchogenic Lung Adenocarcinoma
|
Nonsmall Cell Adenocarcinoma
|
|
Adenocarcinoma Lung
|
Lung Adenocarcinomas
|
|
Non-Small Cell Adenocarcinoma
|
|
|
| Squamous Cell Carcinoma, Head And Neck |
|
Squamous Cell Carcinoma Of The Head And Neck
|
HNSCC
|
|
Head And Neck Squamous Cell Carcinoma
|
Squamous Cell Carcinoma Of Lip
|
|
Squamous Cell Carcinoma, Head And Neck, Somatic
|
Carcinoma Of The Head And Neck
|
|
Squamous Cell Carcinomas Of Head And Neck
|
Scchn
|
|
Squamous Cell Carcinoma Of The Hypopharynx
|
Squamous Cell Carcinoma Of The Oropharynx
|
|
Squamous Cell Carcinoma Of Salivary Glands
|
Squamous Cell Carcinoma Of The Nasal Cavity And Paranasal Sinuses
|
|
Squamous Cell Carcinoma Of The Nasal Cavity And Sinuses
|
Squamous Cell Carcinoma Of The Oral Cavity
|
|
Squamous Cell Carcinoma Of The Lip
|
Carcinoma, Squamous Cell Of Head And Neck
|
|
Lip Squamous Cell Carcinoma
|
Carcinoma, Squamous Cell, Head And Neck
|
|
Salivary Gland Squamous Cell Carcinoma
|
Cancer Of Head And Neck
|
|
Squamous Cell Carcinoma Of Oropharynx Nos
|
|
|
| Cystadenoma |
|
Cystoma
|
Craniopharyngioma
|
|
|
| Papillary Carcinoma |
|
Carcinoma, Papillary
|
Carcinoma Papillary
|
|
|
| Appendix Adenocarcinoma |
|
Cystadenocarcinoma
|
Mucinous Adenocarcinoma
|
|
Adenocarcinoma Of Appendix
|
Appendiceal Adenocarcinoma
|
|
Adenocarcinoma Of The Appendix
|
Colonic Type Adenocarcinoma
|
|
Nonmucinous Adenocarcinoma
|
|
|
| Hypoparathyroidism |
|
Hypoparathyroidism, Idiopathic
|
Parathyroid, Underactivity Of
|
|
Syndrome With Hypoparathyroidism
|
Deficiency Of Parathyroid Hormone
|
|
Parathyroid Gland Insufficiency
|
Parathyroid Insufficiency
|
|
Hypoparathyroidism Due To Impaired Pth - [Parathyroid Hormone] Secretion
|
|
|
| Hypocalcemia, Autosomal Dominant 1 |
|
Autosomal Dominant Hypocalcemia
|
Autosomal Dominant Hypocalcemia 1
|
|
HYPOC1
|
Hypocalcemia, Autosomal Dominant
|
|
Hypercalciuric Hypocalcemia
|
Hypocalcemia, Autosomal Dominant, With Bartter Syndrome
|
|
Familial Hypocalcemia
|
Hypocalcemia, Familial
|
|
Hypoc
|
Adh
|
|
Autosomal Dominant Hypoparathyroidism
|
Familial Hypercalciuric Hypocalcemia
|
|
Ad Hypocalcemia
|
Autosomal Dominant Hypocalcemia With Bartter Syndrome
|
|
Hypoparathyroidism - Autosomal Dominant
|
Hypocalcemia
|
|
|
| Calcinosis |
|
Pathologic Calcification
|
Pathologically Calcified Structure
|
|
|
| Hormone Producing Pituitary Cancer |
|
Growth Hormone Producing Pituitary Tumor
|
Pituitary Tumors, Hormone Producing
|
|
Somatotropinoma
|
Growth Hormone-Producing Pituitary Gland Neoplasm
|
|
|
| Adrenal Adenoma |
|
Adenoma Of The Adrenal Gland
|
Adrenal Incidentaloma
|
|
Adrenal Cortical Adenoma
|
Adrenocortical Adenoma
|
|
|
| Parosteal Osteosarcoma |
|
Juxtacortical Osteosarcoma
|
Parosteal Osteogenic Sarcoma
|
|
Osteosarcoma, Juxtacortical
|
|
|
| Pituitary Cancer |
|
Pituitary Carcinoma
|
Malignant Pituitary Neoplasm
|
|
Malignant Tumor Of Pituitary Gland
|
Neoplasm Of Pituitary Gland
|
|
Pituitary Gland Cancer
|
Pituitary Gland Neoplasm
|
|
Pituitary Neoplasm
|
Carcinoma Of The Pituitary Gland
|
|
Neoplasm Of The Pituitary Gland
|
Pituitary Neoplasms
|
|
Malignant Neoplasm Of Pituitary Gland
|
|
|
| Fibroma |
|
|
| Bartter Syndrome, Type 5, Antenatal, Transient |
|
Bartter Disease Type 5
|
BARTS5
|
|
Bartter Syndrome Type 5
|
Bartter Syndrome Type V
|
|
Transient Antenatal Bartter Syndrome
|
Bartter Syndrome 5, Antenatal, Transient
|
|
|
| Hypophosphatemia |
|
Vitamin D-Resistant Rickets
|
Hereditary Hypophosphatemic Rickets
|
|
Vdrr
|
Vitamin D Resistant Rickets
|
|
Hypophosphatemic Rickets, X-Linked Dominant
|
Familial Hypophosphatemic Rickets
|
|
|
| Follicular Adenoma |
|
Follicular Adenoma Of The Thyroid Gland
|
Thyroid Follicular Adenoma
|
|
Adenoma Follicular
|
Follicular Thyroid Adenoma
|
|
Thyroid Gland Follicular Adenoma
|
|
|
| Metal Metabolism Disorder |
|
Metal Metabolism, Inborn Errors
|
Inborn Metal Metabolism Disorder
|
|
|
| Polyhydramnios |
|
|
| Hypothyroidism |
|
Thyroid Diseases
|
Thyroid Disease
|
|
Thyroid Deficiency
|
Thyroid Insufficiency
|
|
Dysfunction Thyroid
|
Thyroid Dysfunction
|
|
|
| Osteoporosis |
|
Postmenopausal Osteoporosis
|
Osteoporosis, Postmenopausal
|
|
Bone Mineral Density Quantitative Trait Locus
|
Bmnd
|
|
Osteoporosis, Involutional
|
Osteoporosis, Susceptibility To
|
|
Osteoporosis, Postmenopausal, Susceptibility
|
Bone Mineral Density Variation Qtl, Osteoporosis
|
|
OSTEOP
|
Involutional Osteoporosis
|
|
Senile Osteoporosis
|
Osteoporosis Postmenopausal
|
|
Bone Mineral Density, Quantitative Trait Locus
|
Osteoporosis, Senile
|
|
Idiopathic Osteoporosis
|
Bone Rarefaction Nos
|
|
Type 1 Osteoporosis
|
|
|
| Prolactinoma |
|
Prolactin-Producing Pituitary Gland Adenoma
|
Prolactin-Secreting Pituitary Adenoma
|
|
Forbes-Albright Syndrome
|
Lactotroph Adenoma
|
|
Prl-Secreting Pituitary Adenoma
|
Prloma
|
|
Pituitary Lactotrophic Adenoma
|
Familial Prolactinoma
|
|
Pituitary Adenoma, Prolactin-Secreting
|
Prolactinoma Of Pituitary Gland
|
|
PSPA
|
|
|
| Common Bile Duct Neoplasm |
|
Common Bile Duct Neoplasms
|
Neoplasm Of Common Bile Duct
|
|
|
| Chromosome 2q37 Deletion Syndrome |
|
Albright Hereditary Osteodystrophy-Like Syndrome
|
2q37 Microdeletion Syndrome
|
|
Brachydactyly-Intellectual Disability Syndrome
|
Deletion 2q37
|
|
2q37 Deletion Syndrome
|
Brachydactyly-Mental Retardation Syndrome
|
|
Bdmr
|
Albright Hereditary Osteodystrophy Type 3
|
|
Del(2)(Q37)
|
Monosomy 2q37qter
|
|
Albright'S Hereditary Osteodystrophy-Like Syndrome
|
Monosomy 2q37
|
|
Chromosome Deletion Syndrome 2q37
|
|
|
| Colorectal Cancer |
|
Colon Cancer
|
Colorectal Carcinoma
|
|
Colon Carcinoma
|
Colorectal Cancer, Susceptibility To
|
|
Carcinoma Of Colon
|
CRC
|
|
Colorectal Cancer With Chromosomal Instability, Somatic
|
Colon Cancer, Somatic
|
|
Colon Cancer, Susceptibility To
|
Colonic Neoplasms
|
|
Colorectal Neoplasms
|
Colorectal Cancer, Somatic
|
|
Colon Cancer, Advanced, Somatic
|
Colonic Carcinoma
|
|
Colorectal Carcinomas
|
Colon Cancers
|
|
Colorectal Cancers
|
Cancer, Colorectal, Somatic
|
|
Cancer, Colon
|
Cancer, Colorectal, Susceptibility To
|
|
Colorectal Neoplasm
|
Colonic Neoplasm
|
|
Malignant Tumor Of Colon
|
|
|
| Schimmelpenning-Feuerstein-Mims Syndrome |
|
Nevus Sebaceus Of Jadassohn
|
Organoid Nevus Phakomatosis
|
|
Linear Nevus Sebaceous Syndrome
|
Sfm Syndrome
|
|
Jadassohn Nevus Phakomatosis
|
Jnp
|
|
Schimmelpenning Syndrome
|
Solomon Syndrome
|
|
SFM
|
Linear Sebaceous Nevus Syndrome
|
|
Schimmelpenning-Feuerstein-Mims Syndrome, Somatic Mosaic
|
Nevus Sebaceus Syndrome
|
|
Organoid Nevus Syndrome
|
Schimmelpenning Feuerstein Mims Syndrome
|
|
Sebaceous Nevus Syndrome, Linear
|
Epidermal Nevus Syndrome, Formerly
|
|
Sebaceous Nevus Syndrome Linear
|
Linear Nevus Sebaceus Syndrome
|
|
Epidermal Nevus Syndrome
|
Ss
|
|
Nevus Sebaceous
|
|
|
| Carney Complex Variant |
|
Carney Complex
|
Carney Syndrome
|
|
Carney Complex, Type 1
|
Lamb Syndrome
|
|
Name Syndrome
|
Myxoma-Spotty Pigmentation-Endocrine Overactivity Syndrome
|
|
Carney Complex - Trismus - Pseudocamptodactyly Syndrome
|
Carney Complex, Type 2
|
|
Car
|
Cnc1
|
|
Carney Myxoma-Endocrine Complex
|
Myxoma - Spotty Pigmentation - Endocrine Overactivity
|
|
Myxoma, Spotty Pigmentation, And Endocrine Overactivity
|
Lamb - Lentigines, Atrial Myxoma, Mucocutaneous Myoma, Blue Nevus Syndrome
|
|
Name - Nevi, Atrial Myxoma, Skin Myxoma, Ephelides Syndrome
|
Carney Complex-Trismus-Pseudocamptodactyly Syndrome
|
|
CACOV
|
|
|
| Villous Adenoma |
|
Adenoma Villous
|
Adenoma, Villous
|
|
|
| Endometrial Mucinous Adenocarcinoma |
|
Uterine Corpus Mucinous Adenocarcinoma
|
|
|
| Ovarian Cystadenocarcinoma |
|
Cystadenocarcinoma Of Ovary
|
Cystadenocarcinoma Of The Ovary
|
|
|
| Primary Pigmented Nodular Adrenocortical Disease |
|
Ppnad
|
Primary Pigmented Nodular Adrenal Dysplasia
|
|
Pigmented Nodular Adrenocortical Disease, Primary, 2
|
Pigmented Nodular Adrenocortical Disease, Primary, 1
|
|
|
| Lung Cancer |
|
Lung Carcinoma
|
Non-Small Cell Lung Carcinoma
|
|
Lung Cancer, Susceptibility To
|
Lung Cancer, Protection Against
|
|
Adenocarcinoma Of Lung, Somatic
|
Adenocarcinoma Of Lung, Response To Tyrosine Kinase Inhibitor In
|
|
Nonsmall Cell Lung Cancer
|
Lung Neoplasm
|
|
Carcinoma Of Lung
|
Lung Non-Small Cell Carcinoma
|
|
Non-Small Cell Lung Cancer
|
Nsclc
|
|
Lung Neoplasms
|
Malignant Neoplasm Of Lung
|
|
Alveolar Cell Carcinoma
|
Nonsmall Cell Lung Cancer, Somatic
|
|
Nonsmall Cell Lung Cancer, Response To Tyrosine Kinase Inhibitor In
|
Nonsmall Cell Lung Cancer, Susceptibility To
|
|
Lung Cancer, Somatic
|
Lung Cancer, Resistance To
|
|
Cancer Of Lung
|
Cancer Of Bronchus
|
|
Cancer Of The Lung
|
Lung Malignancies
|
|
Lung Malignant Tumors
|
Malignant Lung Tumor
|
|
Malignant Tumor Of Lung
|
Pulmonary Cancer
|
|
Pulmonary Carcinoma
|
Pulmonary Neoplasms
|
|
Respiratory Carcinoma
|
LNCR
|
|
Adenocarcinoma Of Lung
|
Neoplasm Of Lung
|
|
Cancer Lung
|
Carcinoma Non-Small Cell Lung
|
|
Carcinoma, Non-Small-Cell Lung
|
Lung Cancers
|
|
Lung Carcinomas
|
Cancer, Lung
|
|
Cancer, Lung, Non-Small Cell
|
Primary Malignant Neoplasm Of Lung
|
|
Bronchioloalveolar Adenocarcinoma
|
|
|
| Short-Rib Thoracic Dysplasia 13 With Or Without Polydactyly |
|
|
| Hepatocellular Carcinoma |
|
Liver Cancer
|
Primary Liver Cancer
|
|
HCC
|
Hepatoma
|
|
Malignant Neoplasm Of Liver
|
Liver Neoplasms
|
|
Cancer, Hepatocellular
|
Liver Cell Carcinoma
|
|
Lcc
|
Hepatoblastoma, Somatic
|
|
Hepatic Cancer
|
Primary Malignant Neoplasm Of Liver
|
|
Rare Tumor Of Liver And Intrahepatic Biliary Tract
|
Hepatocellular Carcinoma, Somatic
|
|
Hepatocellular Carcinoma, Childhood Type, Somatic
|
Hepatocellular Cancer, Somatic
|
|
Ca Liver - Primary
|
Hepatic Neoplasm
|
|
Malignant Hepato-Biliary Neoplasm
|
Malignant Neoplasm Of Liver, Not Specified As Primary Or Secondary
|
|
Malignant Neoplasm Of Liver, Primary
|
Malignant Tumor Of Liver
|
|
Neoplasm Of Liver
|
Non-Resectable Primary Hepatic Malignant Neoplasm
|
|
Resectable Malignant Neoplasm Of Liver
|
Resectable Malignant Neoplasm Of The Liver
|
|
Primary Liver Carcinoma
|
Primary Malignant Liver Neoplasm
|
|
Primary Cancer Of Liver
|
Primary Tumor Of The Liver
|
|
Rare Tumor Of Liver And Ibt
|
Hepatocellular Cancer
|
|
Neoplasm Of The Liver
|
Carcinoma, Hepatocellular
|
|
Hepatomas
|
Liver Neoplasm
|
|
Liver Carcinoma
|
Liver And Intrahepatic Biliary Tract Carcinoma
|
|
Malignant Hepatobiliary Neoplasm
|
Adult Primary Hepatocellular Carcinoma
|
|
Hepatoblastoma
|
Carcinoma Of Liver
|
|
Malignant Liver Tumour
|
Malignant Hepatic Tumour
|
|
|
| Multiple Enchondromatosis, Maffucci Type |
|
Maffucci Syndrome
|
Chondrodysplasia With Hemangioma
|
|
Chondroplasia Angiomatosis
|
Enchondromatosis With Hemangiomata
|
|
Hemangiomatosis Chondrodystrophica
|
Kast Syndrome
|
|
Multiple Angiomas And Endochondromas
|
Dyschondrodysplasia With Hemangiomas
|
|
Enchondromatosis Type Ii
|
Enchondromatosis With Multiple Cavernous Hemangiomas
|
|
Dyschondroplasia And Cavernous Hemangioma
|
Hemangiomata With Dyschondroplasia
|
|
|
| Temple Syndrome |
|
Uniparental Disomy, Maternal, Chromosome 14
|
Temple Syndrome Due To Paternal 14q32.2 Microdeletion
|
|
Paternal Del(14)(Q32.2)
|
Temple Syndrome Due To Paternal 14q32.2 Hypomethylation
|
|
Temple Syndrome Due To Maternal Uniparental Disomy Of Chromosome 14
|
Upd(14)Mat
|
|
|
| Transient Neonatal Diabetes Mellitus |
|
Diabetes Mellitus, Transient Neonatal
|
Tndm
|
|
Chromosome 6-Associated Transient Diabetes Mellitus
|
Dmtn
|
|
Diabetes Mellitus, 6q24-Related Transient Neonatal
|
Tndm1
|
|
Neonatal Diabetes Mellitus, Transient
|
Tndm -[Transient Neonatal Diabetes Mellitus]
|
|
|
| Basophil Adenoma |
|
Adenoma, Basophil
|
Pituitary Gland Basophilic Adenoma
|
|
|
| Breast Cancer |
|
Breast Carcinoma
|
Male Breast Cancer
|
|
Breast Cancer, Familial
|
Malignant Neoplasm Of Breast
|
|
Breast Cancer, Susceptibility To
|
Breast Cancer, Early-Onset
|
|
Malignant Tumor Of Breast
|
Carcinoma Of Male Breast
|
|
Breast Cancer, Invasive Ductal
|
Breast Cancer, Protection Against
|
|
Breast Cancer, Somatic
|
Breast Cancer, Male
|
|
Breast Cancer, Lobular, Somatic
|
Breast Tumor
|
|
Mammary Cancer
|
Mammary Tumor
|
|
Malignant Neoplasm Of Male Breast
|
Mammary Carcinoma
|
|
Male Breast Carcinoma
|
Familial Cancer Of Breast
|
|
Invasive Ductal Breast Carcinoma
|
Breast Cancer Susceptibility
|
|
Breast Cancer, Male, Susceptibility To
|
Breast Cancer, Early-Onset, Susceptibility To
|
|
Malignant Tumor Of The Breast
|
Mammary Neoplasm
|
|
Primary Breast Cancer
|
Neoplasm Of Male Breast
|
|
Carcinoma Of Breast
|
Breast Cancer In Men
|
|
Familial Breast Cancer
|
Cancer Of Breast
|
|
BC
|
Breast Cancer Familial
|
|
Breast Cancer Familial Male
|
Breast Cancer, Familial Male
|
|
Breast Male Carcinoma
|
Breast Neoplasms
|
|
Breast Neoplasms, Male
|
Mammary Tumors
|
|
Mammary Carcinomas
|
Cancer, Breast
|
|
Cancer, Breast, Susceptibility
|
Invasive Breast Ductal Carcinoma
|
|
Breast Neoplasm
|
Susceptibility To Breast Cancer
|
|
Mammary Neoplasms
|
Animal Mammary Neoplasms
|
|
Primary Malignant Neoplasm Of Breast
|
Infiltrating Ductal Carcinoma Of Breast
|
|
Infiltrating Duct Carcinoma Of Unspecified Site
|
Infiltrating Ductular Carcinoma Of Unspecified Site
|
|
Invasive Breast Carcinoma Of No Special Type
|
Microinvasive Carcinoma Of Breast
|
|
Carcinoma With Apocrine Differentiation
|
|
|
| Osteopetrosis |
|
Marble Bone Disease
|
Albers-Schonberg Disease
|
|
Osteopetroses
|
Marble Bones
|
|
Osteopetrosis And Related Disorders
|
Congenital Osteopetrosis
|
|
Marble Bone
|
Albers-Schoenberg Disease
|
|
Albers-Schonberg Osteopetrosis
|
Osteosclerosis Fragilis
|
|
Ivory Bones
|
|
|
| Precocious Puberty, Male-Limited |
|
Testotoxicosis
|
Familial Male-Limited Precocious Puberty
|
|
Leydig Cell Adenoma, Somatic, With Precocious Puberty
|
FMPP
|
|
Familial Testotoxicosis
|
Sexual Precocity, Familial, Gonadotropin-Independent
|
|
Familial Gonadotropin-Independent Male-Limited Sexual Precocity
|
Male-Limited Precocious Puberty
|
|
Pubertas Praecox
|
Gonadotropin-Independent Familial Sexual Precocity
|
|
Testotoxicosis, Familial
|
Precocious Puberty, Male
|
|
Precocious Puberty, Male Limited
|
Familial Gonadotrophin-Independent Sexual Precocity
|
|
Gipp
|
Gonadotrophin-Independent Precocious Puberty
|
|
Precocious Pseudopuberty
|
Familial Male Precocious Puberty
|
|
Precocious Puberty In Males
|
Puberty, Precocious
|
|
Precocious Puberty
|
|
|
| Juvenile Type Testicular Granulosa Cell Tumor |
|
Juvenile Granulosa Cell Tumor
|
Juvenile Granulosa Cell Tumour
|
|
Juvenile Type Granulosa Cell Neoplasm
|
Juvenile Type Granulosa Cell Tumor
|
|
Juvenile Type Granulosa Cell Tumour
|
Juvenile Type Testicular Granulosa Cell Tumour
|
|
|
| Testicular Granulosa Cell Tumor |
|
Granulosa Cell Tumor Of Testis
|
Granulosa Cell Tumour Of Testis
|
|
Testicular Granulosa Cell Tumour
|
|
|
| Proteus Syndrome |
|
Proteus Syndrome, Somatic
|
Partial Gigantism-Nevi-Hemihypertrophy-Macrocephaly Syndrome
|
|
Gigantism, Partial, Of Hands And Feet, Nevi, Hemihypertrophy, And Macrocephaly
|
Wiedemann'S Syndrome
|
|
Hemihypertrophy And Macrocephaly
|
Partial Gigantism Of Hands And Feet, Nevi, Hemihypertrophy, Macrocephaly
|
|
Ps
|
PROTEUSS
|
|
Partial Gigantism Of Hands And Feet Nevi Hemihypertrophy And Macrocephaly
|
|
|
| Parathyroid Adenoma |
|
Adenoma Of Parathyroid
|
Adenoma Of The Parathyroid Gland
|
|
Parathyroid Gland Adenoma
|
|
|
| Hypertension And Brachydactyly Syndrome |
|
Brachydactyly With Hypertension
|
Bilginturan Syndrome
|
|
HTNB
|
Brachydactyly-Arterial Hypertension Syndrome
|
|
Brachydactyly, Type E, With Short Stature And Hypertension
|
Bilginturan Brachydactyly
|
|
Brachydactyly Type E With Short Stature And Hypertension
|
Type E Brachydactyly With Short Stature And Hypertension
|
|
Brachydactyly Type E, With Short Stature And Hypertension
|
Hypertension With Brachydactyly
|
|
|
| Hyperpituitarism |
|
|
| Phosphorus Metabolism Disease |
|
Phosphorus Metabolism Disorders
|
Disorder Of Phosphorus Metabolism
|
|
Phosphorus Disorder
|
Phosphorus Metabolism Disorder
|
|
|
| Bone Benign Neoplasm |
|
|
| Dicer1 Syndrome |
|
Pleuro-Pulmonary Blastoma Familial Tumor Susceptibility Syndrome
|
Pleuropulmonary Blastoma Familial Tumor Susceptibility Syndrome
|
|
Ppb Familial Tumor Susceptibility Syndrome
|
Dicer1-Related Pleuropulmonary Blastoma Cancer Predisposition Syndrome
|
|
Pleuro-Pulmonary Blastoma Familial Tumor Susceptibility
|
Dicer1-Related Pleuropulmonary Blastoma
|
|
Pleuropulmonary Blastoma Familial Tumor And Dysplasia Syndrome
|
Pleuropulmonary Blastoma Family Tumor Susceptibility Syndrome
|
|
Ppbftds
|
Doid:0081063
|
|
|
| Osteochondrodysplasia |
|
Skeletal Dysplasia
|
Chondrodystrophy
|
|
Congenital Anomaly Of Cartilage
|
Osteochondrodysplasias
|
|
Cartilage Development Disorder
|
Osteochondrodysplasia Syndrome
|
|
Dysplasia, Skeletal
|
Mucopolysaccharidosis Iv
|
|
|
| Silver-Russell Syndrome 1 |
|
Silver-Russell Syndrome
|
Russell-Silver Syndrome
|
|
Silver-Russell Dwarfism
|
Rss
|
|
SRS1
|
Srs
|
|
Silver Russell Dwarfism
|
Russell Silver Syndrome
|
|
Silver Russell Syndrome
|
|
|
| Ovarian Serous Cystadenocarcinoma |
|
Serous Cystadenoma
|
Cystadenoma Serous
|
|
Cystadenoma, Serous
|
|
|
| Functioning Pituitary Adenoma |
|
Secretory Adenoma Of The Pituitary Gland
|
Endocrine Active Pituitary Adenoma
|
|
Secreting Pituitary Adenoma
|
Pituitary Adenoma, Functioning
|
|
|
| Kagami-Ogata Syndrome |
|
Paternal Uniparental Disomy Of Chromosome 14
|
Uniparental Disomy, Paternal, Chromosome 14
|
|
Kos
|
Mca Due To 14q32.2 Maternally Expressed Gene Defect
|
|
Paternal Uniparental Disomy 14
|
Kagami-Ogata Syndrome Due To Maternal 14q32.2 Microdeletion
|
|
Maternal Del(14)(Q32.2)
|
Maternal Monosomy 14q32.2
|
|
Kagami-Ogata Syndrome Due To Maternal 14q32.2 Hypermethylation
|
Kagami-Ogata Syndrome Due To Paternal Uniparental Disomy Of Chromosome 14
|
|
Upd(14)Pat
|
|
|
| Craniosynostosis |
|
Premature Closure Of Cranial Sutures
|
Craniostenosis
|
|
Craniosynostosis Syndrome
|
Cso
|
|
Craniosynostoses
|
Congenital Ossification Of Cranial Sutures
|
|
Congenital Ossification Of Sutures Of Skull
|
Craniostosis
|
|
Imperfect Fusion Of Skull
|
Congenital Imperfect Closure Skull
|
|
Imperfect Closure Skull
|
Premature Closure Cranium Sutures
|
|
Deficiency Of Craniofacial Axis
|
|
|
| Eiken Syndrome |
|
Eiken Skeletal Dysplasia
|
Bone Modeling Defect Of Hands And Feet
|
|
EKNS
|
|
|
| Multiple Endocrine Neoplasia, Type Iv |
|
Multiple Endocrine Neoplasia Type 4
|
MEN4
|
|
Multiple Endocrine Neoplasia 4
|
Neoplasia, Endocrine, Multiple, Type Iv
|
|
|
| Deficiency Anemia |
|
Anemia
|
Deficiency Anemias
|
|
Anaemia
|
|
|
| Mucinous Adenocarcinoma |
|
Mucin-Producing Adenocarcinoma
|
Mucin-Secreting Adenocarcinoma
|
|
Mucin-Secreting Carcinoma
|
Mucous Carcinoma
|
|
Pseudomyxoma Peritonei With Unknown Primary Site
|
Adenocarcinoma, Mucinous
|
|
|
| Enchondromatosis, Multiple, Ollier Type |
|
Ollier Disease
|
Enchondromatosis
|
|
Dyschondroplasia
|
Osteochondromatosis
|
|
Multiple Cartilaginous Enchondroses
|
Multiple Enchondromatosis
|
|
Enchondromatosis With Haemangiomata
|
Enchondromatosis, Multiple
|
|
Kast'S Syndrome
|
Ollier'S Syndrome
|
|
Enchondromatosis Multiple
|
ENCHOM
|
|
Maffucci Disease
|
Olliers Disease
|
|
Hereditary Multiple Exostoses
|
Chondromatosis
|
|
|
| Lissencephaly, X-Linked, 2 |
|
X-Linked Lissencephaly With Abnormal Genitalia
|
Hydranencephaly With Abnormal Genitalia
|
|
Xlag
|
Xlisg
|
|
X-Linked Lissencephaly With Ambiguous Genitalia
|
LISX2
|
|
Lissencephaly, X-Linked 2
|
X-Linked Lissencephaly 2
|
|
X-Linked Lissencephaly-Corpus Callosum Agenesis-Genital Anomalies Syndrome
|
Xlag Syndrome
|
|
Lissencephaly, X-Linked, With Ambiguous Genitalia
|
Xlis2
|
|
X-Linked Lissencephaly - Agenesis Of The Corpus Callosum - Genital Anomalies
|
X-Linked Lissencephaly-Agenesis Of The Corpus Callosum-Genital Anomalies Syndrome
|
|
Xlag Syndrome
|
Lissencephaly X-Linked With Ambiguous Genitalia
|
|
Lissencephaly, X-Linked, Type 2
|
Chromosome Xq26.3 Duplication Syndrome
|
|
|
| Pituitary Gland Disease |
|
Pituitary Diseases
|
Pituitary Dysfunction
|
|
Pituitary Disease
|
Pituitary Deficiency
|
|
Pituitary Disorders
|
|
|
| Ovary Adenocarcinoma |
|
Ovarian Adenocarcinoma
|
Adenocarcinoma Of The Ovary
|
|
Ovarian Adenoacanthoma
|
Adenocarcinoma Of Ovary
|
|
|
| Papillary Adenofibroma |
|
|
| Breast Juvenile Papillomatosis |
|
Juvenile Papillomatosis Of The Breast
|
|
|
| Colon Adenocarcinoma |
|
Adenocarcinoma Of Colon
|
Adenocarcinoma Of The Colon
|
|
Colonic Adenocarcinoma
|
|
|
| Adrenal Gland Disease |
|
Adrenal Gland Diseases
|
Adrenal Gland Disorders
|
|
|
| Dowling-Degos Disease 1 |
|
Reticular Pigment Anomaly Of Flexures
|
DDD1
|
|
Ddd
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Hyperpigmentation
|
|
Dowling-Degos Disease
|
|
|
| Nevus, Epidermal |
|
Epidermal Nevus
|
Woolly Hair Nevus
|
|
Epidermal Naevus
|
Epidermal Nevus Syndrome
|
|
Nevus, Keratinocytic, Nonepidermolytic
|
Epidermal Nevus, Somatic
|
|
Nevus, Epidermal, Somatic
|
Nevus Sebaceous Or Woolly Hair Nevus, Somatic
|
|
Nonepidermolytic Keratinocytic Nevus
|
Epidermal Hamartoma Syndrome
|
|
Wooly Hair Nevus
|
Keratinocytic Non-Epidermolytic Nevus
|
|
KNEN
|
Pigmented Moles
|
|
Organoid Nevus Phakomatosis
|
Nevus Sebaceous
|
|
Melanocytic Nevus
|
Melanocytic Nevus Of Skin
|
|
|
| Thyroid Gland Disease |
|
Abnormality Of The Thyroid Gland
|
Thyroid Diseases
|
|
|
| Beckwith-Wiedemann Syndrome |
|
Wiedemann-Beckwith Syndrome
|
BWS
|
|
Exomphalos-Macroglossia-Gigantism Syndrome
|
Emg Syndrome
|
|
Beckwith-Wiedemann Syndrome Due To Cdkn1c Mutation
|
Emg Abnormality
|
|
Wbs
|
Exomphalos Macroglossia Gigantism Syndrome
|
|
Beckwith-Wiedemann Syndrome Due To Nsd1 Mutation
|
Macroglossia Exomphalos Gigantism
|
|
|
| Bone Osteosarcoma |
|
Osteosarcoma Of Bone
|
Primary Osteosarcoma Of Bone
|
|
|
| Hypertension, Essential |
|
Essential Hypertension
|
Hypertension
|
|
High Blood Pressure
|
Hypertension, Essential, Susceptibility To
|
|
Hypertensive Disease
|
Primary Hypertension
|
|
EHT
|
Hypertension, Salt-Sensitive Essential, Susceptibility To
|
|
Hyperpiesia
|
Idiopathic Hypertension
|
|
Hypertensive Disorder
|
Hypertension, Essential, Susceptibility To, 3
|
|
Hypertension, Essential 3
|
Hypertension, Essential, Salt-Sensitive
|
|
Hypertension, Essential, Susceptibility To, 6
|
Hypertension, Essential 6
|
|
Hypertension, Salt-Sensitive Essential
|
Hypertension, Susceptibility To
|
|
Hypertension, Essential, Susceptibility To, 4
|
Hypertension, Essential 4
|
|
Hypertension, Essential, Susceptibility To, 2
|
Hypertension, Essential 2
|
|
Hypertension, Essential, Susceptibility To, 1
|
Hypertension, Essential 1
|
|
Hypertension, Essential, Susceptibility To, 5
|
Hypertension, Essential 5
|
|
Htn
|
Vascular Hypertensive Disorder
|
|
Systemic Primary Arterial Hypertension
|
Hbp - [High Blood Pressure]
|
|
Systemic Arterial Hypertensive Disorder
|
Elevated Blood Pressure
|
|
Arterial Hypertension Nos
|
Hypertension Nos
|
|
Benign Hypertension
|
Systemic Arterial Hypertension
|
|
Systemic Hypertension
|
Artery Htn
|
|
Benign Htn
|
Vascular Htn
|
|
Vascular Hypertension
|
Cholesterol Hypertension
|
|
Cholesterol Htn
|
Idiopathic Htn
|
|
Malignant Hypertension
|
Malignant Htn
|
|
Raised Blood Pressure
|
Cardiovascular Hypertension
|
|
Primary Htn - [Hypertension]
|
High Arterial Tension
|
|
High Blood Pressure Disorder
|
Ht - [Hypertension]
|
|
Htn - [Hypertension]
|
Hypertensive Vascular Disease
|
|
Hypertensive Vascular Degeneration
|
|
|
| Hemochromatosis, Type 1 |
|
Hemochromatosis
|
Hemochromatosis Type 1
|
|
Hereditary Hemochromatosis
|
Hh
|
|
HFE1
|
Hfe Hemochromatosis, Modifier Of
|
|
Symptomatic Form Of Classic Hemochromatosis
|
Symptomatic Form Of Hemochromatosis Type 1
|
|
Symptomatic Form Of Hfe-Related Hereditary Hemochromatosis
|
Haemochromatosis
|
|
Iron Storage Disorder
|
Bronze Diabetes
|
|
Hereditary Haemochromatosis
|
Hlah
|
|
Hfe
|
Hemochromatosis, Hereditary
|
|
Diabetes Bronze
|
Classic Hemochromatosis
|
|
Hfe-Associated Hereditary Hemochromatosis
|
Hemochromatosis Classic
|
|
Bronzed Cirrhosis
|
Familial Hemochromatosis
|
|
Genetic Hemochromatosis
|
Hc
|
|
Pigmentary Cirrhosis
|
Primary Hemochromatosis
|
|
Troisier-Hanot-Chauffard Syndrome
|
Von Recklenhausen-Applebaum Disease
|
|
Hemochromatosis 1
|
Primary Hereditary Hemochromatosis
|
|
Bronze Cirrhosis
|
|
|
| Lynch Syndrome |
|
Hereditary Nonpolyposis Colon Cancer
|
Hereditary Nonpolyposis Colorectal Cancer
|
|
Hereditary Nonpolyposis Colorectal Carcinoma
|
Hereditary Nonpolyposis Colorectal Neoplasms
|
|
Familial Nonpolyposis Colon Cancer
|
Hnpcc
|
|
Coca 1
|
Hereditary Defective Mismatch Repair Syndrome
|
|
Hereditary Non-Polyposis Colon Cancer
|
Hereditary Non-Polyposis Colon Cancer Syndrome
|
|
Hereditary Non-Polyposis Colorectal Cancer
|
Hereditary Non-Polyposis Colorectal Cancer Syndrome
|
|
Hereditary Nonpolyposis Colon Cancer Syndrome
|
Hereditary Nonpolyposis Colorectal Cancer Syndrome
|
|
Hereditary Nonpolyposis Colorectal Neoplasm
|
Hnpcc - Hereditary Nonpolyposis Colon Cancer
|
|
Cancer Family Syndrome
|
Familial Nonpolyposis Colorectal Cancer
|
|
Colon Cancer, Familial Nonpolyposis
|
Colorectal Neoplasms, Hereditary Nonpolyposis
|
|
Cancer, Colorectal, Nonpolyposis, Hereditary
|
Colorectal Cancer, Hereditary Nonpolyposis, Type 1
|
|
|
