WormBase Tree Display for DO_term: DOID:0111643
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DOID:0111643 | Name | autosomal recessive nonsyndromic deafness 115 | |||
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Status | Valid | ||||
Definition | An autosomal recessive nonsyndromic deafness characterized by onset in early childhood of severe sensorineural hearing impairment that has_material_basis_in homozygous or compound heterozygous mutation in the SPNS2 gene on chromosome 17p13.2. | ||||
Synonym | Exact | DFNB115 | |||
autosomal recessive deafness 115 | |||||
Parent | Is_a | DOID:0050565 | |||
DB_info | Database | OMIM | disease | 618457 | |
Attribute_of | Gene_by_orthology | WBGene00007549 | |||
WBGene00008033 | |||||
WBGene00008598 | |||||
WBGene00013739 |