| Diseases |
Alias |
|
| Isolated Growth Hormone Deficiency, Type Ib |
|
Isolated Growth Hormone Deficiency Type Ib
|
IGHD1B
|
|
Ighd Ib
|
Growth Hormone Deficiency, Isolated, Type Ib
|
|
Congenital Ighd Type Ib
|
Congenital Isolated Gh Deficiency Type Ib
|
|
Congenital Isolated Growth Hormone Deficiency Type Ib
|
Dwarfism Of Sindh
|
|
Pituitary Dwarfism I
|
Isolated Growth Hormone Deficiency Type 1b
|
|
Ighd 1b
|
Growth Hormone Deficiency, Isolated, 1b
|
|
|
| Kowarski Syndrome |
|
Biodefective Growth Hormone
|
Pituitary Dwarfism With Normal Immunoreactive Growth Hormone And Low Somatomedin
|
|
Short Stature Due To Growth Hormone Qualitative Anomaly
|
KWKS
|
|
|
| Isolated Growth Hormone Deficiency, Type Ii |
|
Ighd Ii
|
Isolated Growth Hormone Deficiency Type Ii
|
|
IGHD2
|
Growth Hormone Deficiency, Isolated, Type Ii
|
|
Congenital Ighd Type Ii
|
Congenital Isolated Gh Deficiency Type Ii
|
|
Congenital Isolated Growth Hormone Deficiency Type Ii
|
Pituitary Dwarfism Due To Isolated Growth Hormone Deficiency Autosomal Dominant
|
|
Growth Hormone Deficiency, Isolated, Autosomal Dominant
|
Pituitary Dwarfism Due To Isolated Growth Hormone Deficiency, Autosomal Dominant
|
|
Autosomal Dominant Isolated Growth Hormone Deficiency
|
Autosomal Dominant Pituitary Dwarfism Due To Isolated Growth Hormone Deficiency
|
|
Isolated Growth Hormone Deficiency Type 2
|
Growth Hormone Deficiency, Isolated Autosomal Dominant
|
|
Growth Hormone Deficiency, Isolated, 2
|
Growth Hormone Deficiency Isolated Autosomal Dominant
|
|
|
| Isolated Growth Hormone Deficiency, Type Ia |
|
Ighd Ia
|
Primordial Dwarfism
|
|
Isolated Growth Hormone Deficiency Type Ia
|
Sexual Ateleiotic Dwarfism
|
|
Pituitary Dwarfism I
|
IGHD1A
|
|
Illig-Type Growth Hormone Deficiency
|
Growth Hormone Deficiency, Isolated, Type Ia
|
|
Congenital Ighd Type Ia
|
Congenital Isolated Gh Deficiency Type Ia
|
|
Congenital Isolated Growth Hormone Deficiency Type Ia
|
Pituitary Dwarfism 1
|
|
Growth Hormone Deficiency, Isolated, Autosomal Recessive
|
Autosomal Recessive Isolated Growth Hormone Deficiency
|
|
Isolated Growth Hormone Deficiency Type 1a
|
Congenital Ighd
|
|
Congenital Isolated Gh Deficiency
|
Congenital Isolated Growth Hormone Deficiency
|
|
Growth Hormone Deficiency, Isolated Autosomal Recessive
|
Illig Type Growth Hormone Deficiency
|
|
Non-Acquired Isolated Growth Hormone Deficiency
|
Growth Hormone Deficiency, Isolated, 1a
|
|
Growth Hormone Deficiency Isolated Autosomal Recessive
|
Dwarfism, Primordial
|
|
Dwarfism
|
|
|
| Growth Hormone Deficiency |
|
Somatotropin Deficiency
|
Isolated Somatotropin Deficiency
|
|
|
| Acromegaly |
|
Gigantism
|
Growth Hormone Excess
|
|
Pituitary Giant
|
Somatotroph Adenoma
|
|
Growth Hormone-Secreting Pituitary Adenoma
|
|
|
| Empty Sella Syndrome |
|
Empty Sella Turcica
|
Empty Sella
|
|
|
| Pituitary Gland Disease |
|
Pituitary Diseases
|
Pituitary Dysfunction
|
|
Pituitary Disease
|
Pituitary Deficiency
|
|
Pituitary Disorders
|
|
|
| Laron Syndrome |
|
Growth Hormone Insensitivity Syndrome
|
Growth Hormone Receptor Deficiency
|
|
Laron Dwarfism
|
Pituitary Dwarfism Ii
|
|
Laron-Type Isolated Somatotropin Defect
|
Primary Growth Hormone Resistance
|
|
Laron-Type Dwarfism
|
Laron Type Pituitary Dwarfism I
|
|
Primary Growth Hormone Insensitivity
|
Primary Gh Resistance
|
|
Gh-R Deficiency
|
Growth Hormone Receptor Defect
|
|
Laron-Type Pituitary Dwarfism
|
Laron-Type Short Stature
|
|
Severe Gh Insensitivity
|
Ghis
|
|
Short Stature Due To A Defect In Growth Hormone Receptor Or Post-Receptor Pathway
|
Complete Growth Hormone Insensitivity
|
|
Gh Receptor Deficiency
|
Primary Gh Insensitivity
|
|
Short Stature Due To Growth Hormone Resistance
|
LARS
|
|
|
| Turner Syndrome |
|
Monosomy X
|
Gonadal Dysgenesis Turner Type
|
|
Ullrich-Turner Syndrome
|
Bonnevie-Ullrich Syndrome
|
|
Karyotype 45, X
|
Genital Dwarfism, Turner Type
|
|
Gonadal Dysgenesis
|
45,X
|
|
Turner'S Syndrome
|
Gonadal Dysgenesis - Turner
|
|
Monosomy X Syndrome
|
Xo Syndrome
|
|
Genital Dwarfism
|
45, X Syndrome
|
|
Bonnevie-Ulrich Syndrome
|
Chromosome X Monosomy X
|
|
Schereshevkii Turner Syndrome
|
Turner Varny Syndrome
|
|
Ts
|
45,X Syndrome
|
|
45,X/46,Xx Syndrome
|
Turners Syndrome
|
|
Gonadal Dysgenesis, 45,X
|
X0 Syndrome
|
|
|
| Hypopituitarism |
|
Pituitary Hypofunction
|
Pituitary Insufficiency
|
|
Pituitary Hormone Deficiency
|
Subpituitarism
|
|
Hypophyseal Dystrophy
|
Hypohypophysism
|
|
Anterior Pituitary Insufficiency
|
Deficient Secretion Of One Or More Pituitary Hormones
|
|
Hypopituitarism Syndrome
|
Pituitary Deficiency
|
|
Pituitary Failure
|
Pituitary Insufficiency Nos
|
|
Anterior Pituitary Hypofunction
|
Deficient Secretion Of All Pituitary Hormones
|
|
Hypopituitary Dwarfism
|
Hyposomatotropic Dwarfism
|
|
Hypophyseal Dwarfism
|
Hypopituitary Cachexia
|
|
Hypophyseal Short Stature
|
Panhypopituitarism Syndrome
|
|
Pituitary Cachexia
|
Juvenile Hypopituitarism
|
|
Pituitary Dwarfism
|
Pituitary Gland Hypofunction
|
|
Primary Hypopituitarism
|
Secondary Hypogonadism
|
|
Prepubertal Panhypopituitarism
|
Prepubertal Dwarfism
|
|
Postpartum Panhypopituitary Syndrome
|
Postpartum Hypopituitarism
|
|
Pituitary Short Stature
|
Pituitary Infantilism
|
|
Pituitary Hypogonadism
|
Pituitary Hypoadrenocorticism
|
|
|
| Hyperprolactinemia |
|
Chiari-Frommel Syndrome
|
Hyperprolactinaemia
|
|
Familial Hyperprolactinemia
|
HPRL
|
|
Pregnancy-Related A-G Syndrome
|
Familial Isolated Prolactin Receptor Deficiency
|
|
|
| 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
|
|
|
| Pituitary Tumors |
|
Pituitary Tumor
|
Pituitary Neoplasms
|
|
|
| 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
|
|
|
| Chromophobe Adenoma |
|
Adenoma, Chromophobe
|
Chromophobe Adenoma Of The Pituitary Gland
|
|
Adenoma Chromophobe
|
|
|
| Fibrous Dysplasia |
|
Fibrous Dysplasia Of Bone
|
|
|
| Pituitary Hormone Deficiency, Combined, 2 |
|
Panhypopituitarism
|
Combined Pituitary Hormone Deficiency
|
|
CPHD2
|
Ateliotic Dwarfism With Hypogonadism
|
|
Pituitary Dwarfism Iii
|
Hanhart Dwarfism
|
|
Simmond'S Disease
|
Simmonds' Disease
|
|
Cphd
|
Pituitary Hormone Deficiency, Combined
|
|
Hormone Deficiency, Pituitary, Combined, Type 2
|
Pituitary Dwarfism Type 3
|
|
Sheehan Syndrome
|
|
|
| Hypothalamic Disease |
|
Hypothalamic Diseases
|
Hypothalamic Dysfunction
|
|
Hypothalamic Disorder
|
Hypothalamic Dysfunction Syndromes
|
|
|
| Precocious Puberty |
|
Familial Precocious Puberty
|
Idiopathic Sexual Precocity
|
|
Sexual Precocity
|
Puberty Precocious
|
|
Cryptogenic Sexual Precocity
|
|
|
| Isolated Growth Hormone Deficiency |
|
Congenital Ighd
|
Congenital Isolated Gh Deficiency
|
|
Congenital Isolated Growth Hormone Deficiency
|
Non-Acquired Isolated Growth Hormone Deficiency
|
|
Pituitary Dwarfism
|
Dwarfism, Pituitary
|
|
Isolated Somatotropin Deficiency
|
Isolated Congenital Growth Hormone Deficiency
|
|
Familial Isolated Growth Hormone Deficiency
|
Ighd
|
|
Dwarfism, Growth Hormone Deficiency
|
Growth Hormone Deficiency Dwarfism
|
|
Isolated Gh Deficiency
|
Isolated Hgh Deficiency
|
|
Isolated Human Growth Hormone Deficiency
|
Isolated Somatotropin Deficiency Disorder
|
|
Dwarfism Pituitary
|
|
|
| Adenoma |
|
Acinar Cell Adenoma
|
Adenomas
|
|
Acinic Cell Adenoma
|
|
|
| Anorexia Nervosa |
|
Anorexia Nervosa, Susceptibility To
|
ANON
|
|
Anorexia Nervosa, Susceptibility To, 1
|
An
|
|
Anorexia Nervosa 1
|
An - [Anorexia Nervosa]
|
|
|
| Pituitary Adenoma |
|
Adenoma Of The Pituitary Gland
|
Pituitary Adenomas
|
|
Adenoma, Pituitary
|
Pituitary Gland Adenoma
|
|
Pituitary Neoplasms
|
|
|
| Insulin-Like Growth Factor I |
|
Insulin-Like Growth Factor I Deficiency
|
IGF1 DEFICIENCY
|
|
Insulin-Like Growth Factor I, Resistance To
|
Growth Retardation With Deafness And Mental Retardation Due To Igf1 Deficiency
|
|
Growth Delay Due To Insulin-Like Growth Factor Type 1 Deficiency
|
Growth Delay Due To Insulin-Like Growth Factor I Resistance
|
|
IGF1RES
|
Igf-I Resistance
|
|
Somatomedin, End-Organ Insensitivity To
|
Somatomedin-C
|
|
Somatomedin-C, Resistance To
|
Growth Retardation With Sensorineural Deafness And Mental Retardation
|
|
Insulin-Like Growth Factor 1 Resistance To
|
Igf-1 Resistance
|
|
Somatomedin End-Organ Insensitivity To
|
Somatomedin-C Resistance To
|
|
Growth Restriction With Sensorineural Deafness And Intellectual Disability
|
Growth Delay-Deafness-Intellectual Disability Syndrome
|
|
Growth Delay-Hearing Loss-Intellectual Disability Syndrome
|
Igf-1 Deficiency
|
|
Primary Insulin-Like Growth Factor Deficiency
|
Resistance To Igf-1
|
|
Insulin-Like Growth Factor 1 Resistance
|
End-Organ Insensitivity To Somatomedin
|
|
Igf1 Resistance
|
Resistance To Insulin-Like Growth Factor I
|
|
Resistance To Somatomedin-C
|
Insulin-Like Growth Factor 1, Resistance To
|
|
|
| Pituitary Apoplexy |
|
|
| Hyperthyroidism |
|
|
| 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
|
|
|
| Hypothyroidism, Congenital, Nongoitrous, 4 |
|
Tsh Deficiency
|
CHNG4
|
|
Thyrotropin Deficiency, Isolated
|
Pituitary Cretinism
|
|
Congenital Nongoitrous Hypothyroidism 4
|
Isolated Thyrotropin Deficiency
|
|
Thyroid-Stimulating Hormone Deficiency
|
Hypothyroidism, Congenital, Nongoitrous 4
|
|
Thyroid-Stimulating Hormone, Deficiency Of
|
Isolated Thyroid-Stimulating Hormone Deficiency
|
|
Isolated Tsh Deficiency
|
Hypothyroidism, Congenital, Nongoitrous, Type 4
|
|
Secondary Hypothyroidism
|
Tsh - [Thyroid Stimulating Hormone] Deficiency
|
|
|
| Central Diabetes Insipidus |
|
Neurogenic Diabetes Insipidus
|
Diabetes Insipidus Cranial Type
|
|
Diabetes Insipidus Neurogenic
|
Diabetes Insipidus Neurohypophyseal
|
|
Neurohypophyseal Diabetes Insipidus
|
Pituitary Diabetes Insipidus
|
|
Cdi
|
Doid:0081055
|
|
Diabetes Insipidus
|
Di - [Diabetes Insipidus]
|
|
Adh - [Antidiuretic Hormone Secretion] Deficiency
|
Diabetes Mellitus Insipidus
|
|
Familial Diabetes Insipidus
|
Antidiuretic Hormone Hyposecretion
|
|
Vasopressin Deficiency Syndrome
|
Primary Central Diabetes Insipidus
|
|
Vasopressin Deficiency
|
Vasopressin Hyposecretion
|
|
Diabetes Insipidus Secondary To Vasopressin Deficiency
|
|
|
| Marasmus |
|
Nutritional Marasmus
|
Nutritional Atrophy
|
|
|
| Short Bowel Syndrome |
|
Short Gut Syndrome
|
Acquired Short Bowel Syndrome
|
|
Secondary Short Bowel Syndrome
|
Short Bowel Nos
|
|
|
| Protein-Deficiency Anemia |
|
Anemia Due To Protein Deficiency
|
Protein-Deficiency Anaemia
|
|
Amino-Acid Deficiency Anaemia
|
Anaemia Due To Amino-Acid Disorder
|
|
|
| Polycystic Ovary Syndrome |
|
Polycystic Ovarian Syndrome
|
Pcos
|
|
Polycystic Ovarian Disease
|
Polycystic Ovaries
|
|
Stein-Leventhal Syndrome
|
Multicystic Ovaries
|
|
Polycystic Ovary
|
Sclerocystic Ovaries
|
|
Sclerocystic Ovary Syndrome
|
Stein-Leventhal Synd.
|
|
Cystic Disease Of Ovaries
|
Cystic Disease Of Ovary
|
|
Pco
|
Pcod
|
|
Sclerocystic Ovarian Degeneration
|
Polycystic Ovary Syndrome, Susceptibility To
|
|
Pcos - [Polycystic Ovary Syndrome]
|
Polycystic Ovary Nos
|
|
Pco - [Polycystic Ovary]
|
|
|
| Prader-Willi Syndrome |
|
Prader-Labhart-Willi Syndrome
|
PWS
|
|
Willi-Prader Syndrome
|
Prader-Willi Syndrome Due To Translocation
|
|
Prader-Willi Syndrome Due To Imprinting Mutation
|
Prader-Willi Syndrome Due To Maternal Uniparental Disomy Of Chromosome 15
|
|
Prader Willi Syndrome
|
Upd(15)Mat
|
|
|
| Hyperinsulinism |
|
|
| Hypoglycemia |
|
Hypoglycaemia
|
Low Blood Sugar
|
|
Hypoglycaemia Nos
|
Spontaneous Hypoglycaemia
|
|
Nondiabetic Hypoglycaemia
|
Hypoglycaemic Disorder Nos
|
|
Hypoglycaemic Syndrome
|
|
|
| Glucose Intolerance |
|
Glucose: Intolerance
|
Glucose: Malabsorption
|
|
Malabsorption Of Glucose
|
Impaired Glucose Tolerance
|
|
|
| Premature Ovarian Failure 7 |
|
Adrenocortical Insufficiency
|
POF7
|
|
Adrenal Insufficiency, Nr5a1-Related
|
AINR
|
|
Ovarian Failure, Premature, Type 7
|
Hypoaldosteronism
|
|
Adrenal Cortical Hypofunction
|
Adrenal Failure Nos
|
|
Hypoadrenocorticism
|
Adrenocortical Hypofunction
|
|
Adrenal Cortex Hypofunction
|
Adrenal Cortex Deficiency
|
|
Adrenal Gland Insufficiency
|
Adrenal Hypofunction
|
|
Adrenal Insufficiency
|
Suprarenal Insufficiency
|
|
Corticoadrenal Insufficiency Nos
|
Corticoadrenal Hypofunction
|
|
Corticoadrenal Deficiency
|
Hypoadrenia
|
|
Hypoadrenalism
|
Aldosterone Deficiency
|
|
|
| Uremia |
|
|
| Septooptic Dysplasia |
|
Septo-Optic Dysplasia
|
De Morsier Syndrome
|
|
Growth Hormone Deficiency With Pituitary Anomalies
|
SOD
|
|
Pituitary Hormone Deficiency, Combined, 5
|
Septo-Optic Dysplasia Spectrum
|
|
Septo-Optic Dysplasia With Growth Hormone Deficiency
|
Pituitary Hormone Deficiency, Combined 5
|
|
Hypopituitarism And Septooptic 'Dysplasia'
|
GHDPA
|
|
CPHD5
|
Dysplasia, Septo-Optic
|
|
Kallmann Syndrome
|
|
|
| Hyperandrogenism |
|
Hyperandrogenization Syndrome
|
|
|
| Hypogonadism |
|
|
| Acanthosis Nigricans |
|
|
| Hypothyroidism |
|
Thyroid Diseases
|
Thyroid Disease
|
|
Thyroid Deficiency
|
Thyroid Insufficiency
|
|
Dysfunction Thyroid
|
Thyroid Dysfunction
|
|
|
| Syringomyelia |
|
|
| Vipoma |
|
Wdha Syndrome
|
Pancreatic Cholera
|
|
Pancreatic Vipoma
|
Verner-Morrison Syndrome
|
|
Diarrheogenic Islet Cell Tumor
|
Vip-Secreting Tumor
|
|
Malignant Vasoactive Intestinal Peptide-Secreting Tumor
|
Vasoactive Intestinal Peptide-Secreting Tumor
|
|
Vip- Secreting Tumor
|
Vipoma, Malignant
|
|
Vipoma Syndrome
|
Watery Diarrhea Syndrome
|
|
Watery Diarrhea, Hypokalemia, And Achlorhydria Syndrome
|
Vasoactive Intestinal Peptide Tumor
|
|
Vasoactive Intestinal Peptide-Producing Tumor
|
Watery Diarrhea-Hypokalemia-Achlorhydria Syndrome
|
|
Malignant Vipoma
|
|
|
| Chronic Fatigue Syndrome |
|
Myalgic Encephalomyelitis
|
Postviral Fatigue Syndrome
|
|
Cfs
|
Myalgic Encephalitis
|
|
Encephalomyelitis, Myalgic
|
Chronic Fatigue
|
|
Fatigue Syndrome, Chronic
|
Benign Myalgic Encephalomyelitis
|
|
Akureyri
|
Akureyri Disease
|
|
Cfs - [Chronic Fatigue Syndrome]
|
Epidemic Neuromyasthenia
|
|
Myalgic Encephalomyelitis Syndrome
|
Me - [Myalgic Encephalomyelitis]
|
|
Pvfs - [Postviral Fatigue Syndrome]
|
Neuromyasthenia
|
|
Iceland Disease
|
Icelandic Disease
|
|
|
| Hyperpituitarism |
|
|
| Diabetes Insipidus |
|
|
| Insulinoma |
|
Islet Cell Adenoma
|
Insulin-Producing Tumor Of Islet Cells
|
|
Adenoma Islet Cell
|
Islet Cell Tumor
|
|
Experimental Organism Islet Cell Adenoma Neoplasm
|
|
|
| Type 1 Diabetes Mellitus |
|
Diabetes Mellitus, Insulin-Dependent
|
Diabetes Mellitus Type 1
|
|
IDDM
|
Type 1 Diabetes
|
|
Insulin-Dependent Diabetes Mellitus
|
T1D
|
|
Juvenile-Onset Diabetes
|
Jod
|
|
Diabetes Mellitus, Type 1
|
Diabetes Mellitus, Insulin-Dependent-1
|
|
Type I Diabetes Mellitus
|
Autoimmune Diabetes
|
|
Juvenile Diabetes
|
Juvenile-Onset Diabetes Mellitus
|
|
Diabetes, Insulin Dependent
|
Insulin-Dependent Diabetes Mellitus-1
|
|
Diabetes Mellitus Insulin-Dependent
|
Diabetes Autoimmune
|
|
Diabetes Mellitus, Insulin-Dependent, Susceptibility To
|
Diabetes Mellitus, Type 1, Susceptibility To
|
|
Diabetes Type 1
|
Type I Diabetes
|
|
Diabetes, Autoimmune
|
T1dm - [Type 1 Diabetes Mellitus]
|
|
Iddm - [Insulin Dependent Diabetes Mellitus]
|
Type 1 Iddm
|
|
Juvenile Diabetes Mellitus Without Compications
|
Idiopathic Insulin-Dependent Diabetes Mellitus Without Complications
|
|
Juvenile-Onset Diabetes Mellitus Without Compications
|
Ketosis-Prone Diabetes Mellitus Without Compications
|
|
Juvenile-Onset-Type Diabetes Mellitus Without Compications
|
|
|
| Diencephalic Astrocytoma |
|
Astrocytoma Of Diencephalon
|
|
|
| Hyperglycemia |
|
|
| Pituitary Adenoma 1, Multiple Types |
|
Pituitary Adenoma Predisposition
|
PITA1
|
|
Isolated Familial Somatotropinoma
|
Fis
|
|
Ifs
|
Somatotrophinoma, Familial
|
|
Acromegaly Due To Pituitary Adenoma 1
|
Pagh1
|
|
Pituitary Adenoma 1
|
Somatotropinoma, Familial Isolated
|
|
Somatotropic Adenoma
|
Somatotropinoma
|
|
Pituitary Gigantism
|
Hypophyseal Gigantism
|
|
Infantile And Juvenile Forms Of Acromegaly
|
Acromegaly Due To Pituitary Adenoma
|
|
Familial Isolated Pituitary Adenoma
|
Familial Isolated Somatotropinomas
|
|
Familial Somatotrophinoma
|
Fipa
|
|
Pituitary Adenoma, Growth Hormone-Secreting, 1
|
Gigantism Pituitary
|
|
Pituitary Adenoma, Type 1, Multiple Types
|
Gigantism
|
|
Pituitary Adenoma, Familial Isolated
|
Multiple Gastrointestinal Atresias
|
|
|
| Pituitary-Dependent Cushing'S Disease |
|
Pituitary-Dependent Cushing Disease
|
Pituitary Acth Hypersecretion
|
|
Overproduction Of Acth
|
Pituitary-Dependent Cushings Disease
|
|
Overproduction Of Pituitary Acth
|
Pituitary-Dependent Hyperadrenocorticism
|
|
Corticotroph Pituitary Adenoma
|
Acth- [Adrenocorticotropic Hormone] Secreting Pituitary Adenoma
|
|
Cushing Syndrome Or Disease, Pituitary-Dependent
|
Cushings Basophilism
|
|
Cushing'S Syndrome 3
|
Itsenko-Cushing Syndrome
|
|
Itsenko Disease
|
Pituitary Basophilism
|
|
Pituitary-Dependent Hypercorticalism
|
Suprarenogenic Syndrome
|
|
Cushing Disease
|
Cushing'S Disease
|
|
|
| Craniopharyngioma |
|
Neoplasm Of Rathke'S Pouch
|
Adamantinomatous Tumor
|
|
Craniopharyngeal Duct Tumor
|
Dysodontogenic Epithelial Tumor
|
|
Rathke'S Pouch Tumor
|
|
|
| Prediabetes Syndrome |
|
Prediabetes
|
Impaired Glucose Tolerance
|
|
Prediabetic State
|
IGT
|
|
Igt - [Impaired Glucose Tolerance]
|
Impaired Glucose Tolerance With Unspecified Complication
|
|
Impaired Glucose Tolerance Without Complication
|
Abnormal Glucose Tolerance
|
|
|
| Adermatoglyphia |
|
ADERM
|
Immigration Delay Disease
|
|
Absence Of Fingerprints
|
Adg
|
|
Congenital Absence Of Fingerprints
|
Isolated Congenital Adermatoglyphia
|
|
Fingerprints, Absence Of
|
Skin Abnormalities
|
|
|
| Cystinosis |
|
Cystine Storage Disease
|
Cystine Diathesis
|
|
Cystine Disease
|
Cystinoses
|
|
Protein Defect Of Cystin Transport
|
Cystin Transport, Protein Defect Of
|
|
Nephropathic Cystinosis
|
Protein Defect Of Cystine Transport
|
|
|
| Primary Hyperparathyroidism |
|
Familial Primary Hyperparathyroidism
|
Hyperparathyroidism, Primary
|
|
Hyperparathyroidism Primary
|
Hypocalciuric Hypercalcemia, Familial, Type 1
|
|
Familial Benign Hypercalcemia
|
Familial Hyperparathyroidism
|
|
Parathyroid Enlargement
|
|
|
| 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
|
|
|
| Type 2 Diabetes Mellitus |
|
Insulin Resistance
|
NIDDM
|
|
Type 2 Diabetes
|
Diabetes Mellitus, Non-Insulin-Dependent
|
|
T2D
|
Noninsulin-Dependent Diabetes Mellitus
|
|
Diabetes Mellitus, Type Ii
|
Maturity-Onset Diabetes
|
|
Insulin Resistance, Severe, Digenic
|
Diabetes Mellitus, Type 2
|
|
Diabetes Mellitus, Noninsulin-Dependent
|
Diabetes Mellitus, Noninsulin-Dependent, Association With
|
|
Diabetes Mellitus, Noninsulin-Dependent, Late Onset
|
Hypertension, Insulin Resistance-Related, Susceptibility To
|
|
Insulin Resistance, Susceptibility To
|
Non-Insulin-Dependent Diabetes Mellitus
|
|
Type Ii Diabetes Mellitus
|
Adult-Onset Diabetes Mellitus
|
|
Maturity-Onset Diabetes Mellitus
|
Diabetes Mellitus Type 2
|
|
Type Ii Diabetes
|
Type 2 Diabetes Mellitus, Susceptibility To
|
|
Diabetes, Type 2
|
Diabetes Mellitus, Noninsulin-Dependent, Susceptibility To
|
|
Diabetes Mellitus, Non-Insulin-Dependent, Susceptibility To
|
Diabetes Mellitus, Type 2, Susceptibility To
|
|
Diabetes Mellitus, Noninsulin-Dependent, 2
|
Diabetes Mellitus, Type Ii, Susceptibility To
|
|
Hypertension, Insulin Resistance-Related
|
Adult-Onset Diabetes
|
|
Aodm
|
Diabetes Mellitus, Adult-Onset
|
|
Diabetes Mellitus Type Ii
|
Diabetes Mellitus Type 2, Susceptibility To
|
|
Diabetes, Type Ii, Susceptibility To
|
Diabetes Type 2
|
|
Diabetes Mellitus
|
Adult Onset Diabetes
|
|
Maturity Onset Diabetes
|
Nonketotic Diabetes
|
|
Non-Insulin Dependent Diabetes Mellitus
|
T2dm - [Type 2 Diabetes Mellitus]
|
|
Niddm - [Non Insulin Dependent Diabetes Mellitus]
|
Dm2
|
|
Dm Type Ii
|
Diabetic Type 2
|
|
Insulin Requiring Type 2 Diabetes
|
Noninsulin Dependent Diabetes
|
|
Non-Insulin-Dependent Diabetes Mellitus Without Complications
|
Diabetes Due To Insulin Secretory Defect
|
|
Diabetes Mellitus Due To Insulin Secretory Defect
|
Non-Insulin-Dependent Diabetes Of The Young
|
|
Senile Diabetes
|
Nonketotic Hyperglycaemia
|
|
Stable Diabetes
|
|
|
| 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
|
|
|
| Nickel Allergic Contact Dermatitis |
|
Allergic Contact Dermatitis To Ni
|
|
|
| Sheehan Syndrome |
|
Postpartum Hypopituitarism
|
Sheehan'S Syndrome
|
|
Postpartum Panhypopituitarism
|
Postpartum Panhypopituitary Syndrome
|
|
Postpartum Pituitary Necrosis
|
Simmond'S Disease
|
|
|
| Diabetes Mellitus |
|
|
| Nutritional Deficiency Disease |
|
Malnutrition
|
Nutritional Disorder
|
|
Nutritional Deficiency
|
Nutrition
|
|
Deficiency Diseases
|
Carbamoyl-Phosphate Synthase I Deficiency Disease
|
|
Nutrition Disorders
|
|
|
| Proprotein Convertase 1/3 Deficiency |
|
Obesity Due To Prohormone Convertase I Deficiency
|
Obesity With Impaired Prohormone Processing
|
|
Obesity And Endocrinopathy Due To Impaired Processing Of Prohormones
|
Pci Deficiency
|
|
Proprotein Convertase 1 3 Deficiency
|
Endocrinopathy Due To Proprotein Convertase 1/3 Deficiency
|
|
Proprotein Convertase 1 Deficiency
|
PC1 DEFICIENCY
|
|
|
| Scoliosis |
|
|
| Functioning Pituitary Adenoma |
|
Secretory Adenoma Of The Pituitary Gland
|
Endocrine Active Pituitary Adenoma
|
|
Secreting Pituitary Adenoma
|
Pituitary Adenoma, Functioning
|
|
|
| Van Maldergem Syndrome 1 |
|
Cerebrofacioarticular Syndrome
|
VMLDS1
|
|
Van Maldergem Syndrome
|
Cerebro-Facio-Articular Syndrome
|
|
Van Maldergem Wetzburger Verloes Syndrome
|
|
|
| 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
|
|
|
| Motor Neuron Disease |
|
Anterior Horn Cell Disease
|
Motor Neuron Diseases
|
|
Mnd - [Motor Neurone Disease]
|
Lou Gehrig Disease
|
|
Creeping Palsy
|
Creeping Paralysis
|
|
Bulbar Motor Neuron Disease
|
Bulbar Syndrome
|
|
Anterior Horn Cell Disorder
|
Hereditary Motor Neuron Disease
|
|
|
| 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
|
|
|
| Partial Third-Nerve Palsy |
|
Partial Third Nerve Palsy
|
Third Nerve Palsy With Pupil Sparing
|
|
Third Or Oculomotor Nerve Palsy, Partial
|
Oculomotor Nerve Diseases
|
|
Oculomotor Nerve Paralysis
|
|
|
| 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
|
|
|
| 17-Beta Hydroxysteroid Dehydrogenase Iii Deficiency |
|
17-Ksr Deficiency
|
Neutral 17-Beta-Hydroxysteroid Oxidoreductase Deficiency
|
|
Pseudohermaphroditism, Male, With Gynecomastia
|
17-Beta Hydroxysteroid Dehydrogenase 3 Deficiency
|
|
Testosterone 17-Beta-Dehydrogenase Deficiency
|
17-Ketosteroid Reductase Deficiency Of Testis
|
|
17-Beta-Hydroxysteroid Dehydrogenase 3 Deficiency
|
17-Ketoreductase Deficiency
|
|
17-Ketosteroidreductase Deficiency
|
46,Xy Disorder Of Sex Development Due To 17-Beta-Hydroxysteroid Dehydrogenase 3 Deficiency
|
|
Male Pseudohermaphroditism With Gynecomastia
|
17 Alpha Ksr Deficiency
|
|
17 Alpha Ketosteroid Reductase Deficiency Of Testis
|
17 Beta Hydroxysteroid Dehydrogenase Iii Deficiency
|
|
Male Pseudoherma-Phroditism With Gynecomastia
|
Neutral 17 Beta Hydroxysteroid Oxidoreductase Deficiency
|
|
Male Pseudohermaphrodism With Gynecomastia
|
MPH
|
|
17-Hydroxysteroid Dehydrogenase Deficiency
|
|
|
| Disorder Of Sexual Development |
|
Disorder Of Sex Development
|
Disorders Of Sex Development
|
|
Sex Development Disorder
|
Sex Differentiation Disease
|
|
Dsd
|
Sex Differentiation Disorders
|
|
|
| Deficiency Anemia |
|
Anemia
|
Deficiency Anemias
|
|
Anaemia
|
|
|
| Rasopathy |
|
Ras/Mitogen-Activated Protein Kinase Syndrome
|
|
|
| Noonan Syndrome 1 |
|
Noonan Syndrome
|
NS1
|
|
Male Turner Syndrome
|
Female Pseudo-Turner Syndrome
|
|
Turner Phenotype With Normal Karyotype
|
Noonan Syndrome With Pigmented Villonodular Synovitis
|
|
Turner'S Phenotype, Karyotype Normal
|
Familial Turner Syndrome
|
|
Noonan'S Syndrome
|
Noonan-Ehmke Syndrome
|
|
Ns
|
Pseudo-Ullrich-Turner Syndrome
|
|
Turner Syndrome In Female With X Chromosome
|
Turner-Like Syndrome
|
|
Ullrich-Noonan Syndrome
|
Noonan-Like/Multiple Giant Cell Lesion Syndrome
|
|
Noonan Syndrome-Like Disorder With Multiple Giant Cell Lesions
|
Pterygium Colli Syndrome
|
|
Noonan Syndrome, Type 1
|
Turner Syndrome, Male
|
|
|
