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MIM:615031 - NEUROPATHY, HEREDITARY SENSORY AND AUTONOMIC, TYPE IX, WITH DEVELOPMENTAL DELAY; HSAN9
Xenbase Genes: tecpr2
Human Disease Resource: MIM
| MONDO:0014016 - hereditary spastic paraplegia 49 |
| DOID:0110801 - hereditary spastic paraplegia 49 |
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| MONDO:0014016 - hereditary spastic paraplegia 49 |
| DOID:0110801 - hereditary spastic paraplegia 49 |