ODCs

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2 OMIM references -
3 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Genetic recurrent myoglobinuria

Autosomal dominant spastic paraplegia type 13


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MT-CO1	(0.55)	HSPD1

Citations in the biomedical literature:

Genetic recurrent myoglobinuria		Autosomal dominant spastic paraplegia type 13
	Synonym(s): (no synonyms)		Synonym(s): - SPG13

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Symptoms, signs and abnormal clinical and laboratory findings, not elsewhere classified -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: - Average age of death: - Type of inheritance: autosomal dominant

	External references: 2 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C537485

No signs/symptoms info available.