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1 OMIM reference -
1 associated gene
No signs/symptoms info
PROTEIN INTERACTIONS: 1
1 associated gene
No signs/symptoms info
Connective tissue disorder due to lysyl hydroxylase-3 deficiency
Acute fatty liver of pregnancy

PLOD3 HADHA


INTERACTOME
ASSOCIATIONS

(click on a score value to see the evidence)
PLOD3
(0.49)
HADHA



Citations in the biomedical literature:


Connective tissue disorder due to lysyl hydroxylase-3 deficiency
PLOD3
Acute fatty liver of pregnancy
HADHA



Connective tissue disorder due to lysyl hydroxylase-3 deficiency
Acute fatty liver of pregnancy

Synonym(s):
- Bone fragility-contractures-arterial rupture-deafness syndrome
- Connective tissue disorder due to LH3 deficiency

Synonym(s):
- AFLP

Classification (Orphanet):
- Rare developmental defect during embryogenesis
- Rare genetic disease
- Rare otorhinolaryngologic disease
- Rare systemic or rheumatologic disease
Classification (Orphanet):
- Rare gynecologic or obstetric disease
- Rare hepatic disease

Classification (ICD10):
(no data available)
Classification (ICD10):
- Pregnancy, childbirth and the puerperium -

Epidemiological data:
(no data available)
Epidemiological data:
Class of prevalence: -
Average age onset: adulthood
Average age of death: -
Type of inheritance: multigenic/multifactorial

External references:
1 OMIM reference -
No MeSH references
External references:
No OMIM references
1 MeSH reference: C537957

No signs/symptoms info available.