1 Child Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0111637 | autosomal recessive nonsyndromic deafness 112 | An autosomal recessive nonsyndromic deafness characterized by postlingual progressive sensorineural hearing impairment that has_material_basis_in homozygous or compound heterozygous mutation in the BDP1 gene on chromosome 5q13.2. |
1 Parent Term
| Identifier | Name | Description |
|---|---|---|
| DOID:0050155 | sensory system disease | A nervous system disease which is located in a part of the nervous system responsible for processing sensory information that consists of sensory receptors, neural pathways, and parts of the brain involved in sensory perception. Commonly recognized sensory systems are those for vision, hearing, somatic sensation (touch), taste and olfaction (smell). |
