HSPB8
| Deellabo: | PGD DNA |
| Gen (Gen Code): | HSPB8 |
| Aliases Gen: | H11; HMN2; CMT2L; DHMN2; E2IG1; HMN2A; HSP22 |
| Gen ID (NCBI): | 26353 |
| OMIM Gen ID: | 608014 |
| Chromosomale locatie: | 12q24.23 |
| Genetische aandoening / Analyse: | Neuronopathie, erfelijke distale motorische (HMN2A) |
| OMIM aandoening ID: | 158590 |
| Overerving: | AD |
| Aliases aandoening: | NEURONOPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA; HMN2A HMN IIA NEUROPATHY, DISTAL HEREDITARY MOTOR, TYPE IIA DHMN2A SPINAL MUSCULAR ATROPHY, DISTAL, ADULT, AUTOSOMAL DOMINANT, IIA CHARCOT-MARIE-TOOTH DISEASE, SPINAL, IIA |