ODCs

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1 OMIM reference -
2 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 OMIM reference -
1 associated gene
4 signs/symptoms

Mitochondrial trifunctional protein deficiency

Syndactyly type 3

HADHA	(UniProt - OMIM)		GJA1	(UniProt - OMIM)
HADHB	(UniProt - OMIM)


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

Citations in the biomedical literature:

Mitochondrial trifunctional protein deficiency		Syndactyly type 3
	Synonym(s): - TFP deficiency - TFPD		Synonym(s): - SD3 - Syndactyly of fingers 4 and 5

	Classification (Orphanet): - Inborn errors of metabolism - Rare cardiac disease - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare bone disease - Rare developmental defect during embryogenesis - Rare genetic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: before age 5 Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: D024741		External references: 1 OMIM reference - 1 MeSH reference: C538154

Syndactyly type 3
	Very frequent - Autosomal dominant inheritance - Syndactyly of fingers / interdigital palm Frequent - Camptodactyly of some fingers Occasional - Short foot / brachydactyly of toes
Mitochondrial trifunctional protein deficiency
(no data available)