ODCs

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

PROTEIN INTERACTIONS: 1

2 OMIM references -
2 associated genes
1 sign/symptom

Juvenile Huntington disease

Adenosine monophosphate deaminase deficiency

HTT	(UniProt - OMIM)		AMPD1	(UniProt - OMIM)
			AMPD3	(UniProt - OMIM)


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	HTT	(0.63)	AMPD1

Citations in the biomedical literature:

Juvenile Huntington disease		Adenosine monophosphate deaminase deficiency
	Synonym(s): - JHD - Juvenile Huntington chorea		Synonym(s): - AMP deaminase deficiency - Myoadenylate deaminase deficiency

	Classification (Orphanet): - Rare genetic disease - Rare neurologic disease		Classification (Orphanet): - Inborn errors of metabolism - 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: 1-9 / 1 000 000 Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: Class of prevalence: unknown Average age onset: variable Average age of death: - Type of inheritance: autosomal recessive

	External references: 1 OMIM reference - No MeSH references		External references: 2 OMIM references - 1 MeSH reference: C538234

Adenosine monophosphate deaminase deficiency
	Very frequent - Autosomal recessive inheritance
Juvenile Huntington disease
(no data available)