ODCs

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1 OMIM reference -
1 associated gene
5 signs/symptoms

PROTEIN INTERACTIONS: 1

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

Dyschromatosis symmetrica hereditaria

17q11 microdeletion syndrome


INTERACTOME ASSOCIATIONS (click on a score value to see the evidence)	ADAR	(0.63)	SUZ12

Citations in the biomedical literature:

Dyschromatosis symmetrica hereditaria		17q11 microdeletion syndrome
	Synonym(s): - Acropigmentation of Dohi		Synonym(s): - Del(17)(q11) - Monosomy 17q11 - NF1 microdeletion syndrome - Neurofibromatosis type 1 microdeletion syndrome

	Classification (Orphanet): - Rare genetic disease - Rare skin disease		Classification (Orphanet): - Rare circulatory system disease - Rare developmental defect during embryogenesis - Rare eye disease - Rare genetic disease - Rare neurologic disease - Rare oncologic disease - Rare renal disease - Rare skin disease

	Classification (ICD10): - Diseases of the skin and subcutaneous tissue -		Classification (ICD10): - Congenital malformations, deformations and chromosomal abnormalities -

	Epidemiological data: Class of prevalence: unknown Average age onset: childhood Average age of death: - Type of inheritance: autosomal dominant		Epidemiological data: (no data available)

	External references: 1 OMIM reference - 1 MeSH reference: C535729		External references: 1 OMIM reference - 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
17q11 microdeletion syndrome
(no data available)