ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

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

Hereditary motor and sensory neuropathy, Okinawa type

Hereditary chronic pancreatitis


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	TFG	(0.72)	CFTR

Citations in the biomedical literature:

Hereditary motor and sensory neuropathy, Okinawa type		Hereditary chronic pancreatitis
	Synonym(s): - HMSNP - Hereditary motor and sensory neuropathy, proximal type		Synonym(s): (no synonyms)

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

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

	Epidemiological data: Class of prevalence: unknown Average age onset: - Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant

	External references: 1 OMIM reference - 1 MeSH reference: C535717		External references: 1 OMIM reference - No MeSH references

No signs/symptoms info available.