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Diseases
Genes (1794)
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ASL
Argininosuccinic Aciduria
PMM2
Pmm2 Deficiency
Liver Disease
SLC6A19
Hartnup Disease
POLG
Balo Concentric Sclerosis
Liver Disease
TTPA
Familial Isolated Vitamin E Deficiency
BLM
Bloom Syndrome
SLC17A5
Salla Disease
Liver Disease
OPA3
Costeff Syndrome
IRF6
Van Der Woude Syndrome
Liver Disease
UMOD
Medullary Cystic Kidney Disease
Van Der Woude Syndrome
Liver Disease
MED12
Fg Syndrome
ABCC9
Cantú Syndrome
GRHL3
Van Der Woude Syndrome
IL2RG
X-Linked Severe Combined Immunodeficiency
SYNE1
Bronchopulmonary Dysplasia
Emery–dreifuss Muscular Dystrophy
TNF
Salla Disease
Leptospirosis
Bronchopulmonary Dysplasia
Familial Isolated Vitamin E Deficiency
Van Der Woude Syndrome
Bloom Syndrome
Liver Disease
Systemic Inflammatory Response Syndrome
LMNA
Emery–dreifuss Muscular Dystrophy
Liver Disease
FLNA
Intestinal Neuronal Dysplasia
Bronchopulmonary Dysplasia
Fg Syndrome
Emery–dreifuss Muscular Dystrophy
Liver Disease
NOP56
Spinocerebellar Ataxia Type 36
IL1B
Leptospirosis
Bronchopulmonary Dysplasia
Cystinosis
Van Der Woude Syndrome
Liver Disease
Systemic Inflammatory Response Syndrome