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Diseases
Genes (310)
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MYO5B
Microvillus Inclusion Disease
EZH2
Weaver Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
NSD1
Weaver Syndrome
ALS2
Infantile-Onset Ascending Hereditary Spastic Paralysis
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
CTC1
Cerebroretinal Microangiopathy With Calcifications And Cysts
MC2R
Familial Glucocorticoid Deficiency
IFIH1
Singleton Merten Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
STX3
Microvillus Inclusion Disease
ASS1
Citrullinemia Type I
STN1
Cerebroretinal Microangiopathy With Calcifications And Cysts
CTNS
Cystinosis
EED
Weaver Syndrome
KMT2A
Weaver Syndrome
RB1
Pinealoblastoma
Trilateral Retinoblastoma
MRAP
Familial Glucocorticoid Deficiency