microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability
Microcephaly with or without chorioretinopathy, lymphedema or intellectual disability (MCLID) is a rare autosomal dominant condition characterized by variable expression of microcephaly, ocular disorders including chorioretinopathy, congenital lymphedema of the lower limbs, and mild to moderate intellectual disability. [ Orphanet:2526 ]
Term info
- OMIM:152950 (Orphanet:2526/e)
- DOID:0060349 (MONDO:equivalentTo)
- GARD:0003622 (MONDO:equivalentTo)
- Orphanet:2526 (OMIM:152950)
- UMLS:C1835265 (Orphanet:2526/e)
- MESH:C537711 (Orphanet:2526/e)
ordo_malformation_syndrome
Microcephaly with or without chorioretinopathy, lymphedema or intellectual disability (MCLID) is a rare autosomal dominant condition characterized by variable expression of microcephaly, ocular disorders including chorioretinopathy, congenital lymphedema of the lower limbs, and mild to moderate intellectual disability.
https://omim.org/entry/152950, http://identifiers.org/mesh/C537711, http://purl.obolibrary.org/obo/Orphanet_2526, http://purl.obolibrary.org/obo/DOID_0060349, http://linkedlifedata.com/resource/umls/id/C1835265
chorioretinal dysplasia-microcephaly-mental retardation syndrome, lymphedema and retinal folds with ficrocephaly and microphthalmos, MLCRD, microcephaly, lymphedema, chorioretinal dysplasia syndrome, lymphedema, microcephaly and chorioretinopathy syndrome, microcephaly lymphedema chorioretinal dysplasia, chorioretinal dysplasia-microcephaly-intellectual disability syndrome, microcephaly with or without chorioretinopathy, lymphedema, or intellectual disability, microcephaly with or without chorioretinopathy, lymphedema, or mental retardation
lymphedema, microcephaly, chorioretinopathy syndrome, Mlcrd syndrome, microcephaly and chorioretinopathy with or without intellectual disability, autosomal dominant, lymphedema and retinal Folds with microcephaly and microphthalmos, microcephaly and chorioretinopathy with or without mental retardation, autosomal dominant, Cdmmr syndrome, MCLMR, microcephaly-lymphedema-chorioretinopathy syndrome
MONDO:0007918