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Acute fatty liver of pregnancy
1 associated gene
33 connected diseases
No signs/symptoms info
Disease Type of connection
Mitochondrial trifunctional protein deficiency
Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency
46,XY partial gonadal dysgenesis
Autosomal dominant hypohidrotic ectodermal dysplasia
46,XY complete gonadal dysgenesis
Amyotrophic lateral sclerosis
Autosomal recessive spastic paraplegia type 20
Common variable immunodeficiency
Fibronectin glomerulopathy
Intermittent hydrarthrosis
Leber congenital amaurosis
Senior-Loken syndrome
TRAPS syndrome
Short stature due to isolated growth hormone deficiency with X-linked hypogammaglobulinemia
X-linked agammaglobulinemia
Autosomal recessive cerebellar ataxia - epilepsy - intellectual deficit
Autosomal recessive nonsyndromic sensorineural deafness type DFNB
Craniometaphyseal dysplasia
Dedifferentiated liposarcoma
Estrogen resistance syndrome
Huntington disease
Hypoplastic left heart syndrome
Juvenile Huntington disease
Oculodentodigital dysplasia
Syndactyly type 3
Well-differentiated liposarcoma
Wolf-Hirschhorn syndrome
X-linked Emery-Dreifuss muscular dystrophy
Connective tissue disorder due to lysyl hydroxylase-3 deficiency
Multiple acyl-CoA dehydrogenation deficiency, mild type
Multiple acyl-CoA dehydrogenation deficiency, severe neonatal type
Precursor T-cell acute lymphoblastic leukemia

Classification (Orphanet):
- Rare gynecologic or obstetric disease
- Rare hepatic disease

Classification (ICD10):
- Pregnancy, childbirth and the puerperium -

Epidemiological data:
Class of prevalence: -
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial
External references:
No OMIM references
1 MeSH reference: C537957

Gene symbol UniProt reference OMIM reference
HADHA P40939600890
No signs/symptoms info available.