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 )

Relationships
is a type of: autosomal recessive disease syndrome