| Label | Id | |
|---|---|---|
| CMT1B | 7307 | |
| HMSN1 | 7307 | |
| HMSN1B | 7307 | |
| Hmsn1 | http://purl.obolibrary.org/obo/MONDO_0007307 | |
| Hmsn1B | http://purl.obolibrary.org/obo/MONDO_0007307 | |
| CMT 1B | 7307 | |
| HMSN 1B | 7307 | |
| HMSN IB | 7307 | |
| c6 deficiency | C567307 | |
| autosomal dominant Charcot-Marie-Tooth disease with focally folded myelin sheaths type 1B | 7307 | |
| Charcot Marie Tooth disease type 1B | 7307 | |
| hereditary motor and sensory neuropathy 1 | 7307 | |
| hereditary motor and sensory neuropathy 1B | 7307 | |
| hereditary motor and sensory neuropathy IB | 7307 | |
| SCA8 spinocerebellar ataxia 8 | C537307 |