ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

1 OMIM reference -
2 associated genes
No signs/symptoms info

Fatal infantile hypertonic myofibrillar myopathy

Hereditary sensory and autonomic neuropathy type 5

CRYAB	(UniProt - OMIM)		NGF	(UniProt - OMIM)
			NTRK1	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	CRYAB	(0.49)	NGF

Citations in the biomedical literature:

Fatal infantile hypertonic myofibrillar myopathy		Hereditary sensory and autonomic neuropathy type 5
	Synonym(s): (no synonyms)		Synonym(s): - Congenital insensitivity to pain and thermal analgesia - HSAN5 - NHSA5

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

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

	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: Class of prevalence: <1 / 1 000 000 Average age onset: neonatal/infancy Average age of death: - Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D000699

No signs/symptoms info available.