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Diseases
Genes (1501)
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TTPA
Familial Isolated Vitamin E Deficiency
Metamorphopsia
ATP13A2
Kufor–rakeb Syndrome
Dementia
ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
ITM2B
Retinal Dystrophy With Inner Retinal Dysfunction And Ganglion Cell Abnormalities
Dementia
PQBP1
Pectus Excavatum
Renpenning's Syndrome
ADA2
Sneddon Syndrome
Dementia
BCOR
Pectus Excavatum
Adenoid Cystic Carcinoma
Embryonal Rhabdomyosarcoma
TREM2
Dementia
APP
Dementia
IFIH1
Singleton Merten Syndrome
TP53
Pectus Excavatum
Adenoid Cystic Carcinoma
Embryonal Rhabdomyosarcoma
Dementia
MMP21
Situs Ambiguus
ARID1A
Adenoid Cystic Carcinoma
Embryonal Rhabdomyosarcoma
SETD2
Adenoid Cystic Carcinoma
Embryonal Rhabdomyosarcoma
ACVR2B
Situs Ambiguus
NOTCH3
Pectus Excavatum
Dementia
ZIC3
Situs Ambiguus
PIK3CA
Pectus Excavatum
Adenoid Cystic Carcinoma
Embryonal Rhabdomyosarcoma
Dementia
CREBBP
Pectus Excavatum
Adenoid Cystic Carcinoma