| OBO ID: DOID:0050542 |
| Term Name: | Charcot-Marie-Tooth disease type X | Search Ontology: | |
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| Definition: | A Charcot-Marie-Tooth disease that has_material_basis_in X-linked inheritance of a point mutation in the connexin-32 gene. http://www.ninds.nih.gov/disorders/charcot_marie_tooth/detail_charcot_marie_tooth.htm | ||
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| Ontology: | Human Disease ( DOID:0050542 ) |
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OTHER Charcot-Marie-Tooth disease type X PAGES
GENES INVOLVED
No data available
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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