ODCs

Click node...

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

PROTEIN INTERACTIONS: 1

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

X-linked Opitz G/BBB syndrome

Juvenile Huntington disease


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	MID1	(0.49)	HTT

Citations in the biomedical literature:

X-linked Opitz G/BBB syndrome		Juvenile Huntington disease
	Synonym(s): - X-linked Opitz BBB/G syndrome - X-linked Opitz syndrome - XLOS		Synonym(s): - JHD - Juvenile Huntington chorea

	Classification (Orphanet): - Rare abdominal surgical disease - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare neurologic disease - Rare urogenital disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -		Classification (ICD10): - Diseases of the nervous system -

	Epidemiological data: (no data available)		Epidemiological data: Class of prevalence: 1-9 / 1 000 000 Average age onset: adolescence / young Average age of death: - Type of inheritance: autosomal dominant

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

No signs/symptoms info available.