| Term Name: | dyschromatosis, ichthyosis, deafness, and atopic disease |
|---|---|
| Synonyms: | DIDA |
| 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. |
| Ontology: | Human Disease [DOID:0070723] ( DOID:0070723 ) |