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

Encephalopathy due to hydroxykynureninuria

Charcot-Marie-Tooth disease type 4D


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	KYNU	(0.63)	NDRG1

Citations in the biomedical literature:

Encephalopathy due to hydroxykynureninuria		Charcot-Marie-Tooth disease type 4D
	Synonym(s): - Kynureninase deficiency - Xanthurenic aciduria		Synonym(s): - CMT4D - HMSN, Lom type - Hereditary motor and sensory neuropathy, Lom type

	Classification (Orphanet): - Inborn errors of metabolism - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Endocrine, nutritional and metabolic diseases -		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: no data available 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: 1 OMIM reference - No MeSH references		External references: 1 OMIM reference - 1 MeSH reference: C535716

No signs/symptoms info available.