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Diseases
Genes (611)
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KANK2
Palmoplantar Keratoderma And Woolly Hair
Nephrotic Syndrome, Type 16
ST3GAL3
Epileptic Encephalopathy, Early Infantile, 15
Mental Retardation, Autosomal Recessive 12
COMP
Pseudoachondroplasia
SLC6A19
Hartnup Disease
PAX6
Aniridia 3
SCNN1B
Liddle Syndrome 2
KERA
Cornea Plana 2, Autosomal Recessive
VCP
Inclusion Body Myopathy With Early-Onset Paget Disease With Or Without Frontotemporal Dementia 3
RBM8A
Thrombocytopenia-Absent Radius Syndrome
AHDC1
Xia–gibbs Syndrome
MKS1
Bardet-Biedl Syndrome 11
LZTFL1
Bardet-Biedl Syndrome 11
Unc119 Lipid-Binding Chaperone
SAMD9L
Ataxia-Pancytopenia Syndrome
SAMD9
Tumoral Calcinosis, Normophosphatemic, Familial
CRYBB3
Cataract 22, Multiple Types
COL2A1
Pseudoachondroplasia
Epiphyseal Dysplasia, Multiple, With Myopia And Conductive Deafness
BBS10
Bardet-Biedl Syndrome 11
MAP3K20
Split-Foot Malformation With Mesoaxial Polydactyly
NPHP1
Bardet-Biedl Syndrome 11
Nephronophthisis 16
KIDINS220
Spastic Paraplegia, Intellectual Disability, Nystagmus, And Obesity