ODCs

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

PROTEIN INTERACTIONS: 1

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

Fatal infantile hypertonic myofibrillar myopathy

Multiple myeloma


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CRYAB	(0.7)	CCND1

Citations in the biomedical literature:

Fatal infantile hypertonic myofibrillar myopathy		Multiple myeloma
	Synonym(s): (no synonyms)		Synonym(s): - Kahler's disease - Medullary plasmacytoma - Myelomatosis - Plasma cell myeloma

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

	Classification (ICD10): - Diseases of the nervous system -		Classification (ICD10): - Neoplasms -

	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: (no data available)

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D009101

No signs/symptoms info available.