ODCs

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5 OMIM references -
4 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Familial hemophagocytic lymphohistiocytosis

Charcot-Marie-Tooth disease type 2B1


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	UNC13D	(0.63)	LMNA

Citations in the biomedical literature:

Familial hemophagocytic lymphohistiocytosis		Charcot-Marie-Tooth disease type 2B1
	Synonym(s): - Familial HLH		Synonym(s): - AR-CMT2B1 - Autosomal recessive Charcot-Marie-Tooth disease type 2B1 - Autosomal recessive axonal CMT4C1

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

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

	Epidemiological data: Class of prevalence: unknown Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive		Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal recessive

	External references: 5 OMIM references - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C537990

No signs/symptoms info available.