ODCs

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

PROTEIN INTERACTIONS: 1

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

Distal hereditary motor neuropathy type 2

Congenital factor XIII deficiency


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HSPB1	(0.75)	F13A1

Citations in the biomedical literature:

Distal hereditary motor neuropathy type 2		Congenital factor XIII deficiency
	Synonym(s): - Distal spinal muscular atrophy type 2 - dHMN2 - dSMA2		Synonym(s): - Fibrin-stabilizing factor deficiency

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare hematologic disease

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Diseases of the blood and blood-forming organs and certain disorders involving the immune mechanism -

	Epidemiological data: Class of prevalence: - Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: <1 / 1 000 000 Average age onset: variable Average age of death: - Type of inheritance: autosomal recessive

	External references: 3 OMIM references - No MeSH references		External references: 2 OMIM references - No MeSH references

No signs/symptoms info available.