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Diseases
Genes (679)
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ATP7B
Wilson's Disease
TTPA
Familial Isolated Vitamin E Deficiency
COL2A1
Collagen, Type Ii, Alpha-1
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
SLC20A2
Primary Familial Brain Calcification
PDGFRB
Primary Familial Brain Calcification
UBE3B
Kaufman Oculocerebrofacial Syndrome
RET
Potter Sequence
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
TNF
Diverticulum
Wilson's Disease
Familial Isolated Vitamin E Deficiency
Renpenning's Syndrome
Pleural Effusion
FLNA
Aneurysm Of Sinus Of Valsalva
Intestinal Neuronal Dysplasia
Fg Syndrome
PAH
Phenylketonuria
Wilson's Disease
ITGA8
Potter Sequence
ASS1
Citrullinemia Type I
PDGFB
Primary Familial Brain Calcification
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome