| Diseases |
Alias |
|
| Split-Hand/Foot Malformation 6 |
|
Split Hand-Foot Malformation 6
|
SHFM6
|
|
Ectrodactyly, Autosomal Recessive
|
Ectrodactyly Autosomal Recessive
|
|
Split-Hand/Foot Malformation, Type 6
|
|
|
| Tooth Agenesis, Selective, 8 |
|
STHAG8
|
Selective Tooth Agenesis 8
|
|
|
| Isolated Split Hand-Split Foot Malformation |
|
Ectrodactyly
|
Shfm
|
|
Split Hand Foot Malformation
|
Split-Hand/Foot Malformation
|
|
Split Hand Foot Deformity 1
|
Split Hand Foot Deformity
|
|
|
| Tooth Agenesis |
|
Oligodontia
|
Hypodontia
|
|
Selective Tooth Agenesis
|
Tooth Agenesis, Selective
|
|
Familial Tooth Agenesis
|
Anodontia
|
|
Congenital Absence Of One Tooth
|
|
|
| Split Hand-Foot Malformation |
|
Ectrodactyly
|
Split-Hand/Foot Malformation
|
|
Lobster-Claw Deformity
|
Split-Hand Deformity
|
|
Split Hand Foot Malformation
|
Shfm
|
|
Split Hand Foot Deformity
|
Split Hand Foot Deformity 1
|
|
|
| Fibular Aplasia Or Hypoplasia, Femoral Bowing And Poly-, Syn-, And Oligodactyly |
|
Fuhrmann Syndrome
|
Bowing Of The Femurs, Aplasia Or Hypoplasia Of The Fibula, And Digital Anomalies
|
|
Fibular Hypoplasia Or Aplasia-Femoral Bowing-Oligodactyly Syndrome
|
Fuhrmann-Rieger-De Sousa Syndrome
|
|
FUHRS
|
Fibular Aplasia
|
|
Hypoplasia Femoral Bowing And Poly- Syn- And Oligodactyly
|
|
|
| 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
|
|
|
| Split-Hand/Foot Malformation 4 |
|
SHFM4
|
Split Hand-Foot Malformation 4
|
|
Split-Hand/Foot Malformation, Type 4
|
|
|
| Split-Hand/Foot Malformation 2 |
|
SHFM2
|
Shfd2
|
|
Shsf2
|
Split Hand/Foot Malformation 2
|
|
Split Hand-Foot Malformation 2
|
Split-Hand/Split-Foot Anomaly, X-Linked
|
|
Split-Hand/Foot Deformity 2
|
Split Hand/Foot Malformation X-Linked
|
|
Split Hand Foot Anomaly - X-Linked
|
Split Hand Foot Deformity 2
|
|
|
| Orofacial Cleft 4 |
|
OFC4
|
Cleft Lip With Or Without Cleft Palate, Nonsyndromic, 4
|
|
Nonsyndromic Cleft Lip With Or Without Cleft Palate 4
|
|
|
| Split-Hand/Foot Malformation 3 |
|
SHFM3
|
Split Hand-Foot Malformation 3
|
|
Chromosome 10q24 Duplication Syndrome
|
Shsf3
|
|
Limb Deficiencies, Distal, With Micrognathia
|
Split-Hand/Foot Malformation 3, Gene Duplication Syndrome
|
|
Distal Limb Deficiencies With Micrognathia
|
Limb Deficiencies Distal With Micrognathia
|
|
Buttiens Fryns Syndrome
|
Distal Limb Deficiencies-Micrognathia Syndrome
|
|
10q24 Microduplication Syndrome
|
Buttiens-Fryns Syndrome
|
|
Split-Hand/Foot Malformation, Type 3, Gene Duplication Syndrome
|
|
|
| Tetraamelia Syndrome |
|
Tetra-Amelia Syndrome
|
Tetraamelia-Multiple Malformations Syndrome
|
|
Tetra-Amelia
|
Tetra-Amelia, Autosomal Recessive
|
|
Tetraamelia, Autosomal Recessive
|
Total Amelia
|
|
Zimmer Phocomelia
|
Tetams
|
|
Zimmer Taub Sova Syndrome
|
|
|
| Chromosome 2q35 Duplication Syndrome |
|
Syndactyly
|
Syndactyly Type 1
|
|
Sdty1
|
Zygodactyly
|
|
Syndactyly, Type I
|
Sd1
|
|
Syndactyly, Type 1, With Or Without Craniosynostosis
|
Symphalangism
|
|
Non-Syndromic Syndactyly
|
Symphalangy
|
|
Webbing Of Digits
|
Syndactyly, Type 1
|
|
|
| Osteoporosis-Pseudoglioma Syndrome |
|
OPPG
|
Ops
|
|
Osteoporosis With Pseudoglioma
|
Osteogenesis Imperfecta, Ocular Form
|
|
Ocular Form Of Osteogenesis Imperfecta
|
Osteogenesis Imperfecta Ocular Form
|
|
Osteoporosis Pseudoglioma Syndrome
|
Pseudoglioma With Bone Fragility
|
|
|
| Split-Hand/Foot Malformation 1 With Sensorineural Hearing Loss, Autosomal Recessive |
|
Split Hand-Foot Malformation 1 With Sensorineural Hearing Loss
|
SHFM1D
|
|
Deafness, Congenital, With Split Hands And Feet
|
Split-Hand/Foot Malformation 1 With Sensorineural Hearing Loss
|
|
Congenital Deafness With Split Hands And Feet
|
Split Hand-Split Foot-Deafness Syndrome
|
|
Split Hand-Split Foot-Hearing Loss Syndrome
|
Congenital Deafness And Split Hands And Feet
|
|
Split-Hand/Foot Malformation, Type 1 With Sensorineural Hearing Loss
|
Split-Hand-Foot Malformation With Sensorineural Hearing Loss
|
|
|
| Endosteal Hyperostosis, Autosomal Dominant |
|
Osteosclerosis
|
Worth Syndrome
|
|
Osteosclerosis, Autosomal Dominant
|
Hyperostosis, Endosteal
|
|
Endosteal Hyperostosis, Worth Type
|
Worth Disease
|
|
Autosomal Dominant Endosteal Hyperostosis
|
Autosomal Dominant Osteosclerosis, Worth Type
|
|
Hyperostosis Corticalis Generalisata, Benign Form Of Worth, With Torus Palatinus
|
Autosomal Dominant Osteosclerosis
|
|
Benign Form Of Worth Hyperostosis Corticalis Generalisata With Torus Platinus
|
Worth'S Syndrome
|
|
Worth Type Autosomal Dominant Osteosclerosis
|
Hyperostosis Corticalis Generalisata, Benign Form Of Worth With Torus Palatinus
|
|
Osteosclerosis, Autosomal Dominant, Worth Type
|
WENHY
|
|
Endosteal Hyperostosis Autosomal Dominant
|
Hyperostosis Corticalis Generalisata Benign Form Of Worth With Torus Palatinus
|
|
Osteosclerosis Autosomal Dominant
|
Acquired Osteosclerosis
|
|
|
| Androgenic Alopecia |
|
Androgenetic Alopecia
|
Alopecia Androgenetica, Male Pattern Baldness
|
|
|
| Van Buchem Disease |
|
Hyperostosis Corticalis Generalisata
|
Hyperphosphatasemia Tarda
|
|
VBCH
|
Sost-Related Sclerosing Bone Dysplasia
|
|
Endosteal Hyperostosis Autosomal Recessive
|
Sclerosteosis
|
|
Endosteal Hyperostosis, Autosomal Recessive
|
Hyperotosis Corticalis Generalisata Familiaris
|
|
Sost Sclerosing Bone Dysplasia
|
Smith-Lemli-Opitz Syndrome
|
|
|
| Ectodermal Dysplasia 13, Hair/Tooth Type |
|
ECTD13
|
Ectodermal Dysplasia 13
|
|
|
| Ulna And Fibula, Absence Of, With Severe Limb Deficiency |
|
Schinzel Phocomelia Syndrome
|
Aarrs
|
|
Limb/Pelvis-Hypoplasia/Aplasia Syndrome
|
LPHAS
|
|
Schinzel Type Phocomelia
|
Absence Of Ulna And Fibula With Severe Limb Deficiency
|
|
Al-Awadi/Raas-Rothschild Syndrome
|
Al Awadi-Raas-Rothschild Syndrome
|
|
Al-Awadi/Raas-Rothschild/Schinzel Phocomelia Syndrome
|
Aplasia/Hypoplasia Of Limbs And Pelvis
|
|
Congenital Absence Of Ulna And Fibula
|
Severe Limb Deficit
|
|
Phocomelia, Schinzel Type
|
Al-Awadi-Raas-Rothschild Syndrome
|
|
Ulna And Fibula Absence Of With Severe Limb Deficiency
|
Limb Pelvis Hypoplasia Aplasia Syndrome
|
|
Limb/Pelvis/Uterus-Hypoplasia/Aplasia Syndrome
|
Ulna And Fibula, Absence Of, With Sever Limb Deficiency
|
|
|
| Sclerosteosis |
|
Cortical Hyperostosis With Syndactyly
|
Sost
|
|
Cortical Hyperostosis-Syndactyly Syndrome
|
|
|
| Pancreatic Cancer |
|
Pancreatic Carcinoma
|
Carcinoma Of Pancreas
|
|
Familial Pancreatic Carcinoma
|
Pancreatic Neoplasm
|
|
Pancreatic Carcinoma, Familial
|
Malignant Neoplasm Of Pancreas
|
|
Pancreatic Acinar Carcinoma
|
Pancreatic Tumor
|
|
Familial Pancreatic Cancer
|
Neoplasm Of The Pancreas
|
|
Cancer Of The Pancreas
|
Pancreatic Carcinoma, Somatic
|
|
Pancreatic Cancer, Somatic
|
Ca Body Of Pancreas
|
|
Ca Head Of Pancreas
|
Ca Tail Of Pancreas
|
|
Malignant Neoplasm Of Body Of Pancreas
|
Malignant Neoplasm Of Head Of Pancreas
|
|
Malignant Neoplasm Of Tail Of Pancreas
|
Pancreas Neoplasm
|
|
Exocrine Cancer
|
Exocrine Pancreas Carcinoma
|
|
Hereditary Pancreatic Cancer
|
Hereditary Pancreatic Carcinoma
|
|
PNCA
|
Pancreatic Cancer, Susceptibility To
|
|
Carcinoma Of Head Of Pancreas
|
Pancreatic Neoplasms
|
|
Pancreatic Tumors
|
Cancer, Pancreatic
|
|
Cancer Of Pancreas
|
Mixed Islet Cell With Exocrine Carcinoma Of Unspecified Site
|
|
|
| Exudative Vitreoretinopathy |
|
Familial Exudative Vitreoretinopathy
|
Fevr
|
|
Criswick-Schepens Syndrome
|
Exudative Vitreoretinopathy, Familial
|
|
Vitreoretinopathy, Exudative )
|
Exudative Vitreoretinopathy 1
|
|
|
| Robinow Syndrome |
|
Acral Dysostosis With Facial And Genital Abnormalities
|
Fetal Face Syndrome
|
|
Robinow Dwarfism
|
Mesomelic Dwarfism-Small Genitalia Syndrome
|
|
Robinow-Silverman-Smith Syndrome
|
Costovertebral Segmentation Defect With Mesomelia
|
|
Covesdem Syndrome
|
Robinow'S Syndrome
|
|
Robinow-Silverman Syndrome
|
|
|
| Gastric Cancer |
|
Stomach Cancer
|
Gastric Carcinoma
|
|
Stomach Carcinoma
|
Gastric Cancer, Somatic
|
|
Gastric Neoplasm
|
Carcinoma Of Stomach
|
|
Stomach Neoplasms
|
Malignant Neoplasm Of Stomach
|
|
Gastric Cancer Risk After H. Pylori Infection
|
Cancer Of The Stomach
|
|
Adult Stomach Cancer
|
Adult Stomach Carcinoma
|
|
GASC
|
Gastric Cancer Intestinal
|
|
Gastric Cancers
|
Gastric Carcinomas
|
|
Cancer, Gastric
|
Stomach Neoplasm
|
|
Malignant Neoplasm Of Body Of Stomach
|
Malignant Tumor Of Lesser Curve Of Stomach
|
|
Gastrocarcinoma Of Unspecified Site
|
Leather Bottle Stomach
|
|
Carcinoma Of Fundus Of Stomach
|
Cancer Of Fundus Of Stomach
|
|
Primary Malignant Neoplasm Of Body Of Stomach
|
Cancer Of Body Of Stomach
|
|
Primary Malignant Neoplasm Of Pyloric Antrum
|
Pyloric Antrum Cancer
|
|
Malignant Tumour Of Stomach
|
|
|
| Ectodermal Dysplasia 10b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive |
|
Hypohidrotic Ectodermal Dysplasia
|
Hed
|
|
Anhidrotic Ectodermal Dysplasia
|
Ectodermal Dysplasia, Hypohidrotic
|
|
Eda
|
Christ-Siemens-Touraine Syndrome
|
|
ECTD10B
|
Ectodermal Dysplasia Anhidrotic
|
|
Ectodermal Dysplasia, Anhidrotic
|
Cst Syndrome
|
|
Ectodermal Dysplasia Hypohidrotic Autosomal Recessive
|
Dysplasia, Ectodermal, Type 10b, Hypohidrotic/Hair/Tooth, Autosomal Recessive
|
|
Dysplasia, Ectodermal, Hypohidrotic
|
Ectodermal Dysplasia 11b, Hypohidrotic/Hair/Tooth Type, Autosomal Recessive
|
|
Ectodermal Dysplasia 3, Anhidrotic
|
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive
|
|
|
| Norrie Disease |
|
Atrophia Bulborum Hereditaria
|
Episkopi Blindness
|
|
Pseudoglioma
|
ND
|
|
Norrie-Warburg Disease
|
Anderson-Warburg Syndrome
|
|
Fetal Iritis Syndrome
|
Norrie Syndrome
|
|
Norrie-Warburg Syndrome
|
Ndp
|
|
Congenital Progressive Oculo-Acoustico-Cerebral Degeneration
|
Norrie'S Disease
|
|
Oligophrenia Microphthalmus
|
Pseudoglioma Congenita
|
|
Whitnall-Norman Syndrome
|
|
|
| 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
|
|
|
| Cleft Palate, Isolated |
|
Cleft Palate
|
Isolated Cleft Palate
|
|
CPI
|
Cp
|
|
Palatoschisis
|
Cleft Palate Isolated
|
|
Uranostaphyloschisis
|
Congenital Fissure Of Palate
|
|
Cleft Of Secondary Palate
|
|
|
| Brittle Bone Disorder |
|
Osteogenesis Imperfecta
|
Brittle Bone Disease
|
|
Fragilitas Ossium
|
Osteopsathyrosis
|
|
Lobstein Disease
|
Oi
|
|
Vrolik Disease
|
Lobstein'S Disease
|
|
Lobstein'S Syndrome
|
Vrolik'S Disease
|
|
Porak And Durante Disease
|
Glass Bone Disease
|
|
Osteogenesis Imperfecta, Dominant Perinatal Lethal
|
Osteogenesis Imperfecta, Recessive Perinatal Lethal
|
|
Brittle Bone Syndrome
|
Oi - [Osteogenesis Imperfecta]
|
|
Ossium Fragility
|
Osteitis Fragilitans
|
|
Bony Fragility
|
Blue Sclera With Fragility Of Bone And Deafness
|
|
White Blue Sclera - Fragility Of Bone - Deafness
|
|
|
