| Diseases |
Alias |
|
| Cone-Rod Dystrophy 15 |
|
Retinitis Pigmentosa 65
|
CORD15
|
|
Dystrophy, Cone-Rod, Type 15
|
|
|
| Ectodermal Dysplasia, Ectrodactyly, And Macular Dystrophy Syndrome |
|
Eem Syndrome
|
Ectodermal Dysplasia, Ectrodactyly, And Macular Dystrophy
|
|
EEMS
|
Ectodermal Dysplasia-Ectrodactyly-Macular Dystrophy Syndrome
|
|
Albrectsen-Svendsen Syndrome
|
Ohdo-Hirayama-Terawaki Syndrome
|
|
Dysplasia, Ectodermal, Ectrodactyly, And Macular Dystrophy
|
|
|
| Autosomal Dominant Intellectual Developmental Disorder 19 |
|
Autosomal Dominant Non-Syndromic Intellectual Disability 19
|
Autosomal Dominant Mental Retardation 19
|
|
Mrd19
|
|
|
| Elsahy-Waters Syndrome |
|
Brachioskeletogenital Syndrome
|
Bsg Syndrome
|
|
Branchioskeletogenital Syndrome
|
ESWS
|
|
Hypospadias, Hypertelorism, Upper Lid Coloboma, And Mixed-Type Hearing Loss
|
Branchio-Skeleto-Genital Syndrome
|
|
|
| Gastric Adenocarcinoma |
|
Adenocarcinoma Of Stomach
|
Stomach Adenocarcinoma
|
|
Adenocarcinoma Gastric
|
Intestinal Type Adenocarcinoma Of Unspecified Site
|
|
Diffuse Type Adenocarcinoma Of Unspecified Site
|
|
|
| Agenesis Of Corpus Callosum, Cardiac, Ocular, And Genital 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
|
|
|
| Cleft Lip/Palate-Ectodermal Dysplasia Syndrome |
|
Orofacial Cleft 7
|
Zlotogora-Ogur Syndrome
|
|
CLPED1
|
Ectodermal Dysplasia, Margarita Island Type
|
|
Ed4
|
Cleft Lip-Palate-Ectodermal Dysplasia Syndrome
|
|
Cleft Lip/Palate-Syndactyly-Pili Torti Syndrome
|
Syndactyly-Ectodermal Dysplasia-Cleft/Lip Palate
|
|
Ectodermal Dysplasia 4
|
Ectodermal Dysplasia Margarita Type
|
|
Ectodermal Dysplasia, Type 4
|
Ectodermal Dysplasia, Cleft Lip And Palate, Mental Retardation, And Syndactyly
|
|
Margarita Type Of Ectodermal Dysplasia
|
Zlotogora-Zilberman-Tenenbaum Syndrome
|
|
Ectd4
|
Ectodermal Dysplasia 4, Hair/Nail Type
|
|
EDMI
|
Ectodermal Dysplasia Type 4
|
|
Margarita Island Ectodermal Dysplasia
|
Syndactyly-Ectodermal Dysplasia-Cleft Lip/Palate
|
|
Non-Syndromic Orofacial Cleft 7
|
OFC7
|
|
Non-Syndromic Cleft Lip/Palate 7
|
Non-Syndromic Cleft Lip With Or Without Cleft Palate 7
|
|
|
| Developmental And Epileptic Encephalopathy 9 |
|
Efmr
|
Epileptic Encephalopathy, Early Infantile, 9
|
|
Eiee9
|
DEE9
|
|
Juberg-Hellman Syndrome
|
Epilepsy, Female-Restricted, With Mental Retardation
|
|
Developmental And Epileptic Encephalopathy, 9
|
Early Infantile Epileptic Encephalopathy 9
|
|
Early Infantile Female-Limited Epilecptic Encephalopathy
|
Female Restricted Epilepsy With Mental Retardation
|
|
Juberg Hellman Syndrome
|
Pcdh19-Related Female-Limited Epilepsy
|
|
Epilepsy And Intellectual Disability Limited To Females
|
Epilepsy, Female Restricted, With Intellectual Disability
|
|
Familial Epilepsy And Intellectual Disability Limited To Females
|
Female Restricted Epilepsy With Intellectual Delays
|
|
Pcdh19-Related Fle
|
Pcdh19-Related Infantile Epileptic Encephalopathy
|
|
Female Restricted Epilepsy With Intellectual Disability
|
Encephalopathy, Epileptic, Early Infantile, Type 9
|
|
|
| Ritter'S Disease |
|
Staphylococcal Scalded Skin Syndrome
|
Pemphigus Neonatorum
|
|
Ritter Disease
|
Dermatitis Exfoliativa Neonatorum
|
|
Scalded Skin Syndrome
|
Toxic Epidermal Necrolysis, Subcorneal Type
|
|
Generalized Exfoliative Disease
|
Ssss
|
|
Ssss - [Staphylococcal Scalded Skin Syndrome]
|
|
|
| Usher Syndrome, Type I |
|
USH1
|
Usher Syndrome Type 1
|
|
Us1
|
Usher Syndrome, Type 1b
|
|
Usher Syndrome Type 1e
|
Retinitis Pigmentosa And Congenital Deafness
|
|
Usher Syndrome, Type Ie
|
USH1E
|
|
Usher Syndrome, Type 1e
|
Usher Syndrome, Type 1a
|
|
Usher Syndrome, Type Ib
|
Usher Syndrome Type 1b
|
|
Usher Syndrome Type Ie
|
Usher Syndrome Type I
|
|
Usher 1
|
Usher Syndrome, Type 1
|
|
Ush1a
|
Usher Syndrome, Type I, French Variety
|
|
Usher Syndrome, Type Ia
|
Usher Syndrome 1b
|
|
USH1B
|
Usher'S Syndrome Type 1b
|
|
Usher Syndrome Type Ib
|
Ushib
|
|
|
| Retinitis Pigmentosa 55 |
|
RP55
|
Retinitis Pigmentosa, Type 55
|
|
|
| Usher Syndrome, Type If |
|
Usher Syndrome Type 1f
|
USH1F
|
|
Usher Syndrome, Type 1f
|
Usher Syndrome Type If
|
|
Usher Syndrome 1f
|
Usher'S Syndrome Type 1f
|
|
|
| Usher Syndrome, Type Id |
|
Usher Syndrome Type 1d
|
USH1D
|
|
Usher Syndrome, Type 1d
|
Usher Syndrome Type Id
|
|
Usher Syndrome, Type Id/F, Digenic
|
Usher Syndrome, Type 1d/F Digenic
|
|
Usher Syndrome 1d
|
Usher'S Syndrome Type 1d
|
|
Usher Syndrome 1d/F
|
USH1DF
|
|
Ush1d/F
|
Usher'S Syndrome Type 1h
|
|
Usher Syndrome 1h
|
Usher Syndrome Type Ih
|
|
Usher Syndrome, Type 1d/F
|
|
|
| Diffuse Gastric And Lobular Breast Cancer Syndrome |
|
Hereditary Diffuse Gastric Cancer
|
HDGC
|
|
LBC
|
Familial Diffuse Gastric Cancer
|
|
Fdgc
|
Hereditary Diffuse Gastric Adenocarcinoma
|
|
Breast Cancer, Lobular
|
Gastric Cancer, Familial Diffuse, And Cleft Lip With Or Without Cleft Palate
|
|
DGLBC
|
Gastric Cancer, Hereditary Diffuse
|
|
Gastric Cancer, Familial Diffuse Breast Cancer, Lobular
|
Diffuse Gastric And Lobular Breast Cancer Syndrome With Or Without Cleft Lip And/Or Palate
|
|
E-Cadherin-Associated Hereditary Gastric Cancer
|
Familial Diffuse Cancer Of Stomach
|
|
Hereditary Diffuse Cancer Of Stomach
|
Gastric Cancer Familial Diffuse
|
|
Gastric Cancer Familial Diffuse And Cleft Lip With Or Without Cleft Palate
|
Cancer, Gastric, Hereditary Diffuse
|
|
|
| Diffuse Gastric Cancer |
|
Hereditary Diffuse Gastric Adenocarcinoma
|
Hereditary Diffuse Gastric Cancer
|
|
Signet Cell Adenocarcinoma
|
Signet Ring Cell Carcinoma
|
|
Signet Ring Cell Gastric Carcinoma
|
Signet Ring Gastric Carcinoma
|
|
Fdgc
|
Familial Diffuse Cancer Of Stomach
|
|
Familial Diffuse Gastric Cancer
|
Gastric Cancer, Familial Diffuse
|
|
Gastric Cancer, Hereditary Diffuse
|
Hdgc
|
|
Hereditary Diffuse Cancer Of Stomach
|
Diffuse Gastric Cancer Syndrome
|
|
Cancer, Gastric, Diffuse
|
Carcinoma, Signet Ring Cell
|
|
Gastric Signet Ring Carcinoma
|
|
|
| Deafness, Autosomal Recessive 12 |
|
DFNB12
|
Deafness, Autosomal Recessive 12, Modifier Of
|
|
Autosomal Recessive Nonsyndromic Deafness 12
|
Autosomal Recessive Deafness 12
|
|
Deafness, Autosomal Recessive, 12
|
Congenital Neurosensory Deafness Autosomal Recessive 12
|
|
Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 12
|
Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 12
|
|
Deafness, Autosomal Recessive, Type 12
|
|
|
| Deafness, Autosomal Recessive 23 |
|
DFNB23
|
Autosomal Recessive Nonsyndromic Deafness 23
|
|
Autosomal Recessive Deafness 23
|
Deafness, Autosomal Recessive, 23
|
|
Non-Syndromic Neurosensory Deafness Autosomal Recessive Type 23
|
Non-Syndromic Sensorineural Deafness Autosomal Recessive Type 23
|
|
Deafness, Autosomal Recessive, Type 23
|
|
|
| Exudative Vitreoretinopathy 7 |
|
EVR7
|
Vitreoretinopathy, Exudative 7
|
|
Vitreoretinopathy Exudative, Type 7
|
|
|
| Pemphigus Vulgaris, Familial |
|
Pemphigus Vulgaris
|
Familial Pemphigus Vulgaris
|
|
Pemphigus
|
|
|
| Van Maldergem Syndrome |
|
Van Maldergem Wetzburger Verloes Syndrome
|
Cerebro-Facio-Articular Syndrome
|
|
Cerebro-Facio-Articular Syndrome Of Van Maldergem
|
Cerebrofacioarticular Syndrome
|
|
Cerebro Facio Articular Syndrome
|
Van Maldergem-Wetzburger-Verloes Syndrome
|
|
|
| Craniofacial-Deafness-Hand Syndrome |
|
CDHS
|
Craniofacial Deafness Hand Syndrome
|
|
Sommer-Young-Wee-Frye Syndrome
|
Features Of Flat Facial Profile, Hypertelorism, Hypoplastic Nose With Slitlike Nares, And A Sensorineural Hearing Loss
|
|
Craniofacial-Hearing Loss-Hand Syndrome
|
|
|
| Bullous Skin Disease |
|
Skin Diseases Bullous
|
Skin Diseases, Bullous
|
|
|
| Adult Liposarcoma |
|
|
| 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
|
|
|
| Blepharocheilodontic Syndrome 1 |
|
Blepharocheilodontic Syndrome
|
Bcd Syndrome
|
|
Elschnig Syndrome
|
Clefting, Ectropion, And Conical Teeth
|
|
Lagophthalmia With Bilateral Cleft Lip And Palate
|
Blepharo-Cheilo-Odontic Syndrome
|
|
Bcds
|
Ectropion, Inferior, With Cleft Lip And/Or Palate
|
|
Blepharo-Cheilo-Dontic Syndrome
|
BCDS1
|
|
Ectropion Inferior Cleft Lip And Or Palate
|
Clefting-Ectropion-Conical Teeth Syndrome
|
|
Ectropion Inferior-Cleft Lip And/Or Palate Syndrome
|
Lagophthalmia-Cleft Lip And Palate Syndrome
|
|
Blepharocheilodontic Syndrome, Type 1
|
|
|
| Breast Lobular Carcinoma |
|
Cancer, Breast, Lobular
|
Lobular Breast Carcinoma
|
|
|
| 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
|
|
|
| Cri-Du-Chat Syndrome |
|
5p Deletion Syndrome
|
5p Partial Monosomy Syndrome
|
|
Monosomy 5p
|
Cat Cry Syndrome
|
|
Chromosome 5p Deletion Syndrome
|
Cri Du Chat Syndrome
|
|
5p- Syndrome
|
5p Minus Syndrome
|
|
Chromosome 5p- Syndrome
|
Chromosome 5 Short Arm Deletion Syndrome
|
|
Chromosome 5p Deletion
|
Deletion 5p
|
|
Cri Du Chat
|
5p Partial Deletion Syndrome
|
|
Partial Deletion Of Short Arm Of Chromosome 5 Syndrome
|
|
|
| Familial Woolly Hair Syndrome |
|
Wooly Hair
|
Familial Wooly Hair Syndrome
|
|
Hereditary Woolly Hair Syndrome
|
Hereditary Wooly Hair Syndrome
|
|
Woolly Hair
|
Syndrome With Woolly Hair
|
|
Wooly Hair Syndrome
|
|
|
| Spinocerebellar Ataxia 45 |
|
SCA45
|
Spinocerebellar Ataxia Type 45
|
|
|
| Usher Syndrome |
|
Deafness-Retinitis Pigmentosa Syndrome
|
Dystrophia Retinae Pigmentosa-Dysostosis Syndrome
|
|
Graefe-Usher Syndrome
|
Hallgren Syndrome
|
|
Usher'S Syndrome
|
Retinitis Pigmentosa-Deafness Syndrome
|
|
Retinitis Pigmentosa-Hearing Loss Syndrome
|
Ush
|
|
Usher Syndromes
|
|
|
| Van Maldergem Syndrome 1 |
|
Cerebrofacioarticular Syndrome
|
VMLDS1
|
|
Van Maldergem Syndrome
|
Cerebro-Facio-Articular Syndrome
|
|
Van Maldergem Wetzburger Verloes Syndrome
|
|
|
| Autosomal Recessive Nonsyndromic Deafness |
|
Deafness, Autosomal Recessive, Nonsyndromic
|
|
|
| Periventricular Nodular Heterotopia |
|
Periventricular Heterotopia
|
Pvnh
|
|
Familial Nodular Heterotopia
|
Heterotopia, Periventricular
|
|
Periventricular Heterotopia, X-Linked
|
|
|
| Hirschsprung Disease 1 |
|
Hirschsprung Disease
|
Aganglionic Megacolon
|
|
Hscr
|
Hirschsprung'S Disease
|
|
Congenital Megacolon
|
Congenital Intestinal Aganglionosis
|
|
Colonic Aganglionosis
|
Hirschsprung Disease, Susceptibility To, 1
|
|
Hirschsprung Disease, Protection Against
|
HSCR1
|
|
Mgc
|
Pelvirectal Achalasia
|
|
Total Intestinal Aganglionosis
|
Megacolon, Aganglionic
|
|
Macrocolon
|
Hscr 1
|
|
Hirschsprung Disease Type 1
|
Hirschsprung Disease, Type 1
|
|
Congenital Dilatation Of Colon
|
Aganglionosis
|
|
Congenital Aganglionic Megacolon
|
Aganglionosis Of Colon
|
|
Bowel Aganglionosis
|
Colon Aganglionosis
|
|
Hirschsprung Megacolon
|
|
|
| Congenital Nervous System Abnormality |
|
Congenital Neurologic Anomaly
|
Congenital Nervous System Disorder
|
|
|
| Nervous System Disease |
|
Abnormality Of The Nervous System
|
Nervous System Diseases
|
|
Nervous System Disorder
|
|
|
| Cone-Rod Dystrophy 2 |
|
Cone-Rod Dystrophy
|
CORD2
|
|
Cone-Rod Retinal Dystrophy
|
Rcrd2
|
|
Cone-Rod Retinal Dystrophy 2
|
Crd2
|
|
Cord
|
Crd
|
|
Retinal Cone-Rod Dystrophy
|
Cone-Rod Retinal Dystrophy-2
|
|
Retinal Cone-Rod Dystrophy 2
|
Tapetoretinal Degeneration
|
|
Cone-Rod Degeneration
|
Cone Rod Dystrophy
|
|
Dystrophy, Cone-Rod
|
Dystrophy, Cone-Rod, Type 2
|
|
Retinitis Pigmentosa
|
Retinitis Pigmentosa 2
|
|
Progressive Cone-Rod Dystrophy
|
|
|
| Fundus Dystrophy |
|
Retinal Dystrophy
|
Retinal Dystrophies
|
|
Dystrophy, Retinal
|
|
|
| Retinitis Pigmentosa |
|
RP
|
Rod-Cone Dystrophy
|
|
Autosomal Recessive Retinitis Pigmentosa
|
Non-Syndromic Retinitis Pigmentosa
|
|
Pericentral Pigmentary Retinopathy
|
Pigmentary Retinopathy
|
|
Tapetoretinal Degeneration
|
Rcd
|
|
Retinitis Pigmentosa Autosomal Recessive
|
ARRP
|
|
Retinitis Pigmentosa, Autosomal Recessive
|
Retinitis Pigmentosa 1
|
|
|
