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Diseases
Genes (719)
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MYO5B
Microvillus Inclusion Disease
ABHD5
Cerebral Creatine Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
MC2R
Familial Glucocorticoid Deficiency
PITX3
Anterior Segment Dysgenesis 1
HLA-DRB1
Heck's Disease
Sarcoidosis, Susceptibility To, 1
BTNL2
Sarcoidosis, Susceptibility To, 1
ALPL
Hypophosphatasia, Childhood
COX4I2
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, And Calvarial Hyperostosis
STX3
Microvillus Inclusion Disease
FOXE3
Anterior Segment Dysgenesis 1
ANXA11
Sarcoidosis, Susceptibility To, 1
MRAP
Familial Glucocorticoid Deficiency
PXDN
Anterior Segment Dysgenesis 1
IL18
Sarcoidosis, Susceptibility To, 1
FOXI1
Enlarged Vestibular Aqueduct
KCNJ10
Enlarged Vestibular Aqueduct
SLC26A4
Enlarged Vestibular Aqueduct
WWTR1
Epithelioid Hemangioendothelioma
CAMTA1
Epithelioid Hemangioendothelioma