microcephaly with or without chorioretinopathy, lymphedema, or mental retardation

Summary
Synonym
  • chorioretinal dysplasia-microcephaly-mental retardation syndrome
  • lymphedema and retinal folds with ficrocephaly and microphthalmos
  • lymphedema, microcephaly and chorioretinopathy syndrome
  • microcephaly lymphedema chorioretinal dysplasia
  • microcephaly, lymphedema, chorioretinal dysplasia syndrome
Definition
A syndrome characterized by variable expression of microcephaly, ocular disorders including chorioretinopathy, congenital lymphedema of the lower limbs, and mild to moderate intellectual disability.
Super Class
autosomal dominant disease syndrome
Disease Ontology
DOID:0060349
Mondo Disease Ontology
MeSH
UMLS
ORDO
OMIM
Related Genes
Displaying 1 entry
Gene ID Gene Symbol Description Source
3832 KIF11 kinesin family member 11

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Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: December 9, 2024