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Diseases
Genes (1032)
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ASL
Argininosuccinic Aciduria
TTPA
Familial Isolated Vitamin E Deficiency
PMM2
Pmm2 Deficiency
F12
Factor Xii Deficiency
MED12
Squamous-Cell Carcinoma Of The Lung
Fg Syndrome
TNFAIP3
Haploinsufficiency Of A20
SLC12A6
Andermann Syndrome
PQBP1
Renpenning's Syndrome
SLC17A5
Salla Disease
FAM20A
Enamel-Renal Syndrome
ACVR2B
Heterotaxy, Visceral, 7, Autosomal
NGLY1
Ngly1 Deficiency
UBE3B
Kaufman Oculocerebrofacial Syndrome
IFIH1
Singleton Merten Syndrome
BRAF
Squamous-Cell Carcinoma Of The Lung
Erdheim–chester Disease
Factor Xii Deficiency
ACTG2
Berdon Syndrome
MMP21
Heterotaxy, Visceral, 7, Autosomal
FGFR2
Squamous-Cell Carcinoma Of The Lung
FLNA
Intestinal Neuronal Dysplasia
Fg Syndrome
TRNL1
Merrf Syndrome