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Diseases
Genes (415)
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ARSL
Brachytelephalangic Chondrodysplasia Punctata
X-Linked Chondrodysplasia Punctata 1
MED12
Raynaud-Claes Syndrome
Fg Syndrome
TTPA
Familial Isolated Vitamin E Deficiency
PEX7
Rhizomelic Chondrodysplasia Punctata Type 1
SLC12A6
Andermann Syndrome
PQBP1
Renpenning's Syndrome
SLC17A5
Salla Disease
FAM20A
Enamel-Renal Syndrome
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
IQSEC2
Raynaud-Claes Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Berdon Syndrome
NKX2-6
Persistent Truncus Arteriosus
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
PLXND1
Persistent Truncus Arteriosus
DLG3
Renpenning's Syndrome
Raynaud-Claes Syndrome
ASS1
Citrullinemia Type I
MYH11
Berdon Syndrome
MYLK
Berdon Syndrome