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Diseases
Genes (744)
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ATP7B
Wilson's Disease
TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
SLC20A2
Cyclopia
Primary Familial Brain Calcification
FAM20A
Enamel-Renal Syndrome
PDGFRB
Primary Familial Brain Calcification
UBE3B
Kaufman Oculocerebrofacial Syndrome
RET
Potter Sequence
IFIH1
Singleton Merten Syndrome
TNF
Wilson's Disease
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Pleural Effusion
FLNA
Aneurysm Of Sinus Of Valsalva
Intestinal Neuronal Dysplasia
Fg Syndrome
ITGA8
Potter Sequence
ASS1
Citrullinemia Type I
SHH
Cyclopia
Potter Sequence
PDGFB
Primary Familial Brain Calcification
ANXA5
Wilson's Disease
ALAD
Lead Poisoning
FREM1
Unibrow
Potter Sequence
CTNS
Cystinosis