ODCs

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1 OMIM reference -
1 associated gene
No signs/symptoms info

PROTEIN INTERACTIONS: 1

1 associated gene
No signs/symptoms info

Autosomal recessive spastic paraplegia type 20

Acute fatty liver of pregnancy


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	SPG20	(0.72)	HADHA

Citations in the biomedical literature:

Autosomal recessive spastic paraplegia type 20		Acute fatty liver of pregnancy
	Synonym(s): - Childhood-onset spastic paraparesis - distal muscle wasting - SPG20 - Troyer syndrome		Synonym(s): - AFLP

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

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Pregnancy, childbirth and the puerperium -

	Epidemiological data: Class of prevalence: - Average age onset: - Average age of death: - Type of inheritance: autosomal recessive		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.