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Syndactyly type 3

1 OMIM reference -
1 associated gene
4 signs/symptoms

PROTEIN INTERACTIONS: 1

Acute fatty liver of pregnancy

1 associated gene
No signs/symptoms info

Syndactyly type 3

Acute fatty liver of pregnancy

(UniProt - OMIM)

(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	GJA1	(0.63)	HADHA

Citations in the biomedical literature:

Syndactyly type 3		Acute fatty liver of pregnancy
	Synonym(s): - SD3 - Syndactyly of fingers 4 and 5		Synonym(s): - AFLP

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

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Pregnancy, childbirth and the puerperium -

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: - Average age onset: adulthood Average age of death: - Type of inheritance: multigenic/multifactorial

	External references: 1 OMIM reference - 1 MeSH reference: C538154		External references: No OMIM references 1 MeSH reference: C537957

Syndactyly type 3
	Very frequent - Autosomal dominant inheritance - Syndactyly of fingers / interdigital palm Frequent - Camptodactyly of some fingers Occasional - Short foot / brachydactyly of toes
Acute fatty liver of pregnancy
(no data available)