OBO ID: DOID:0110169 |
Term Name: | Charcot-Marie-Tooth disease axonal type 2P | Search Ontology: | |
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Definition: | A Charcot-Marie-Tooth disease type 2 that has_material_basis_in homozygous or heterozygous mutation in the LRSAM1 gene on chromosome 9q33. https://www.ncbi.nlm.nih.gov/pubmed/20865121 | ||
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Ontology: | Human Disease ( DOID:0110169 ) |
OTHER Charcot-Marie-Tooth disease axonal type 2P PAGES
ZEBRAFISH MODELS
No data available
PHENOTYPE
No data available
CITATIONS: None
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