ODCs

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4 associated genes
No signs/symptoms info

PROTEIN INTERACTIONS: 1

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

Pediatric systemic lupus erythematosus

Hereditary sensory and autonomic neuropathy type 5


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	PTPN22	(0.68)	NTRK1

Citations in the biomedical literature:

Pediatric systemic lupus erythematosus		Hereditary sensory and autonomic neuropathy type 5
	Synonym(s): - SLE, pediatric onset		Synonym(s): - Congenital insensitivity to pain and thermal analgesia - HSAN5 - NHSA5

	Classification (Orphanet): - Rare neurologic disease - Rare renal disease - Rare respiratory disease - Rare systemic or rheumatologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the musculoskeletal system and connective tissue -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: (no data available)		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: No OMIM references No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: D000699

No signs/symptoms info available.