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Diseases
Genes (636)
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TTPA
Familial Isolated Vitamin E Deficiency
PQBP1
Renpenning's Syndrome
SLC20A2
Cyclopia
Primary Familial Brain Calcification
MED12
Fg Syndrome
SLC17A5
Salla Disease
FAM20A
Enamel-Renal Syndrome
PDGFRB
Primary Familial Brain Calcification
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
RET
Potter Sequence
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
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
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome
CTNS
Cystinosis