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Summary Literature (0)
DOID:0060349 - microcephaly with or without chorioretinopathy, lymphedema, or mental retardation

Disease Ontology 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.

Synonyms: 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,

Xenbase Genes : kif11

Mondo Disease Ontology (on Monarch Initiative):
MONDO:0007918 - microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability

Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD

Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s): autosomal dominant disease (is_a), syndrome (is_a)