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Diseases
Genes (475)
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MYO15A
Deafness, Autosomal Recessive 3
TTPA
Familial Isolated Vitamin E Deficiency
AGL
Glycogen Storage Disease Type Iii
PIK3CD
Activated Pi3k Delta Syndrome
PQBP1
Renpenning's Syndrome
PHKG2
Glycogen Storage Disease Type Ix
Phosphorylase Kinase Deficiency
Glycogen Storage Disease Ixc
SLC20A2
Primary Familial Brain Calcification
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
PDGFRB
Primary Familial Brain Calcification
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
FLNA
Aneurysm Of Sinus Of Valsalva
Intestinal Neuronal Dysplasia
Fg Syndrome
ASS1
Citrullinemia Type I
PDGFB
Primary Familial Brain Calcification
GRIN2A
Rolandic Epilepsy
CTNS
Cystinosis
PHKA2
Glycogen Storage Disease Type Ix
Phosphorylase Kinase Deficiency
Glycogen Storage Disease Ixc
RB1
Pinealoblastoma
Trilateral Retinoblastoma
PIK3R1
Activated Pi3k Delta Syndrome