WormBase Tree Display for DO_term: DOID:0081274
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| DOID:0081274 | Name | peroxisome biogenesis disorder 14B | |||
|---|---|---|---|---|---|
| Status | Valid | ||||
| Definition | A peroxisome biogenesis disorder that is characterized clinically by mild intellectual disability, congenital cataracts, progressive hearing loss, and polyneuropathy and that has_material_basis_in homozygous mutation in the PEX11B gene on chromosome 1q21. | ||||
| Parent | Is_a | DOID:0050737 | |||
| DOID:0080377 | |||||
| DB_info | Database | OMIM | disease | 614920 |
