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Hao-Fountain syndrome due to USP7 mutation

MedGen UID:: 1054565
•Concept ID:: CN377631
•: Disease or Syndrome

Synonym:	USP7-related neurodevelopmental disorder

Gene (location): Gene(s) directly associated with this condition or phenotype.	USP7 (16p13.2)

Monarch Initiative:	MONDO:0958071
OMIM®:	616863

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GTR
MeSH

CClinical test, RResearch test, OOMIM, GGeneReviews, VClinVar

CROGVHao-Fountain syndrome
- CROGVHao-Fountain syndrome due to 16p13.2 microdeletion
- CROGVHao-Fountain syndrome due to USP7 mutation

Partial deletion of the short arm of chromosome 16
- Hao-Fountain syndrome
  - Hao-Fountain syndrome due to USP7 mutation

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Hao-Fountain syndrome due to USP7 mutation
Hao-Fountain syndrome due to USP7 mutation

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