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Diseases
Genes (971)
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ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
SMAD4
Congenital Contractural Arachnodactyly
Juvenile Polyposis Syndrome
FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
BMPR1A
Juvenile Polyposis Syndrome
BRAF
Congenital Contractural Arachnodactyly
Langerhans Cell Histiocytosis
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
GALE
Galactose Epimerase Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
ACTG2
Congenital Contractural Arachnodactyly
Berdon Syndrome
CFH
Membranoproliferative Glomerulonephritis
MYH11
Juvenile Polyposis Syndrome
Aneurysm
Berdon Syndrome
ENG
Juvenile Polyposis Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
MYLK
Aneurysm
Berdon Syndrome
ASS1
Argininosuccinic Aciduria
Congenital Contractural Arachnodactyly
Citrullinemia Type I