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Human Disease and Mouse Model Detail
Human Disease Axenfeld-Rieger Anomaly with Partially Absent Eye Muscles, Distinctive Face, Hydrocephaly, and Skeletal Abnormalities
OMIM ID: 109120
Human Phenotype Ontology associations
Synonyms De Hauwere Syndrome; Iris Dysplasia with Ocular Hypertelorism, Psychomotor Retardation, and Sensorineural Deafness
Genes and
mouse models
There are currently no human or mouse genes associated with this disease in the MGI database.

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