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Human Disease and Mouse Model Detail
Human Disease Linear Skin Defects with Multiple Congenital Anomalies 1; LSDMCA1
OMIM ID: 309801
Human Phenotype Ontology associations
Synonyms Linear Skin Defects with Multiple Congenital Anomalies; Microphthalmia with Linear Skin Defects; MLS; Microphthalmia, Dermal Aplasia, and Sclerocornea; Microphthalmia, Syndromic; Microphthalmia, Syndromic 7; MCOPS7; Midas Syndrome
View all models View ALL (9) mouse models for this human disease.
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
     HCCS* Hccs* View 3 models HomoloGene
     ARHGAP6 Arhgap6* View 3 models HomoloGene and HGNC
MID1 Mid1* View 3 models HomoloGene
References Disease References using Mouse Models (1)

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 6.05
The Jackson Laboratory