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Human Disease and Mouse Model Detail
Human Disease Microcephaly with or without Chorioretinopathy, Lymphedema, or Mental Retardation; MCLMR
OMIM ID: 152950
Human Phenotype Ontology associations
Synonyms Cdmmr Syndrome; Lymphedema and Retinal Folds with Microcephaly and Microphthalmos; Lymphedema, Microcephaly, Chorioretinopathy Syndrome; Microcephaly and Chorioretinopathy with or without Mental Retardation, Autosomal Dominant; Microcephaly, Lymphedema, Chorioretinal Dysplasia Syndrome; Mlcrd Syndrome
Genes and
mouse models
Mutations in human and/or mouse homologs are associated with this disease

      *Disease is associated/modeled with this Gene or a homolog. More...
      Human Homologs Mouse Homologs Mouse Models Homology Source
     KIF11* Kif11   HomoloGene and HGNC

Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Tumor Biology (MTB), Gene Ontology (GO), MouseCyc
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last database update
MGI 6.07
The Jackson Laboratory