ODCs

Click node...

1 OMIM reference -
1 associated gene
5 signs/symptoms

COMMON GENES: 1

2 OMIM references -
3 associated genes
No signs/symptoms info

Dyschromatosis symmetrica hereditaria

Familial infantile bilateral striatal necrosis

Citations in the biomedical literature:

Dyschromatosis symmetrica hereditaria		Familial infantile bilateral striatal necrosis
	Synonym(s): - Acropigmentation of Dohi		Synonym(s): - Familial IBSN - Familial infantile striatonigral degeneration - Familial infantile striatonigral necrosis

	Classification (Orphanet): - Rare genetic disease - Rare skin disease		Classification (Orphanet): - Rare genetic disease - Rare neurologic disease

	Classification (ICD10): - Diseases of the skin and subcutaneous tissue -		Classification (ICD10): - Diseases of the nervous system -

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

	External references: 1 OMIM reference - 1 MeSH reference: C535729		External references: 2 OMIM references - No MeSH references

Dyschromatosis symmetrica hereditaria
	Very frequent - Irregular / in bands / reticular skin hyperpigmentation - Irregular / patchy skin hypopigmentation - Macules Frequent - Autosomal recessive inheritance - Dystonia / torticollis / writer's cramp / blepharospasms
Familial infantile bilateral striatal necrosis
(no data available)