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Diseases
Genes (365)
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MYO5B
Microvillus Inclusion Disease
TTPA
Familial Isolated Vitamin E Deficiency
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
PQBP1
Renpenning's Syndrome
MC2R
Familial Glucocorticoid Deficiency
IFIH1
Hepatitis E
Singleton Merten Syndrome
STX3
Microvillus Inclusion Disease
CD55
Protein Losing Enteropathy
TFE3
Epithelioid Hemangioendothelioma
Vascular Tumor
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency
WWTR1
Epithelioid Hemangioendothelioma
CAMTA1
Epithelioid Hemangioendothelioma
IL6
Hepatitis E
Fibrous Dysplasia Of Bone
Lumbar Disc Disease
Aseptic Meningitis
Familial Isolated Vitamin E Deficiency
YAP1
Epithelioid Hemangioendothelioma
CILP
Lumbar Disc Disease
DDX58
Hepatitis E
Singleton Merten Syndrome
STAR
Adrenal Crisis
Familial Glucocorticoid Deficiency
COL9A3
Lumbar Disc Disease
SART3
Disseminated Superficial Actinic Porokeratosis