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Diseases
Genes (952)
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BRAF
Congenital Contractural Arachnodactyly
Langerhans Cell Histiocytosis
Erdheim–chester Disease
ASL
Argininosuccinic Aciduria
FBN2
Congenital Contractural Arachnodactyly
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
PQBP1
Renpenning's Syndrome
MED12
Fg Syndrome
FAM20A
Enamel-Renal Syndrome
UBE3B
Kaufman Oculocerebrofacial Syndrome
GALE
Galactose Epimerase Deficiency
IFIH1
Singleton Merten Syndrome
ACTG2
Congenital Contractural Arachnodactyly
Berdon Syndrome
CFH
Membranoproliferative Glomerulonephritis
MYH11
Aneurysm
Berdon Syndrome
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
MYLK
Aneurysm
Berdon Syndrome
ASS1
Argininosuccinic Aciduria
Congenital Contractural Arachnodactyly
Citrullinemia Type I
TSLP
Membranoproliferative Glomerulonephritis
CTNS
Cystinosis
SLC4A4
Proximal Renal Tubular Acidosis