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Metadata
ID DOID:0081442
Name blepharophimosis-impaired intellectual development syndrome
Definition A syndrome that is characterized by a distinct facial appearance with blepharophimosis and global development delay and that has_material_basis_in heterozygous mutation in the SMARCA2 gene on chromosome 9p24.
https://pubmed.ncbi.nlm.nih.gov/32694869/
Xrefs

MIM:619293

ORDO:637013

Subsets

DO_rare_slim

Synonyms

SMARCA2-related blepharophimosis-intellectual disability syndrome [EXACT]

Parent Relationships

is_a syndrome

is_a autosomal dominant disease

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