dyschromatosis, ichthyosis, deafness, and atopic disease Disease Ontology Browser

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Disease Ontology Browser

dyschromatosis, ichthyosis, deafness, and atopic disease (DOID:0070723)
Alliance: disease page
Synonyms: DIDA
Alt IDs: OMIM:621400
Definition: A syndrome characterized by generalized hyperpigmentation with hypopigmented spots, ichthyosis, sensorineural hearing loss, atopic dermatitis, asthma, and allergic rhinitis that has_material_basis_in compound heterozygous mutation in the OSBPL2 gene on chromosome 20q13.

Contributing Projects: Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB)), Gene Ontology (GO)
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