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Diseases
Genes (729)
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ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
ACVR2B
Heterotaxy, Visceral, 7, Autosomal
UBE3B
Kaufman Oculocerebrofacial Syndrome
BCOR
Embryonal Rhabdomyosarcoma
Adenoid Cystic Carcinoma
IFIH1
Singleton Merten Syndrome
MMP21
Heterotaxy, Visceral, 7, Autosomal
ARID1A
Embryonal Rhabdomyosarcoma
Adenoid Cystic Carcinoma
Nasopharyngeal Carcinoma
FLNA
Intestinal Neuronal Dysplasia
Nasopharyngeal Carcinoma
Fg Syndrome
SETD2
Embryonal Rhabdomyosarcoma
Adenoid Cystic Carcinoma
TP53
Embryonal Rhabdomyosarcoma
Adenoid Cystic Carcinoma
Tenosynovial Giant Cell Tumor
Nasopharyngeal Carcinoma
ASS1
Argininosuccinic Aciduria
Citrullinemia Type I
ZIC3
Heterotaxy, Visceral, 7, Autosomal
LEFTY2
Heterotaxy, Visceral, 7, Autosomal
CTNS
Cystinosis
PIK3CA
Embryonal Rhabdomyosarcoma
Adenoid Cystic Carcinoma
Nasopharyngeal Carcinoma