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Term ID: | 8051 |
Name: | NF1 Microduplication Syndrome |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D008607|MESH:D017253|MESH:D019066|MESH:D025063|MESH:D058674 |
TreeNumbers: | C04.557.580.600.580.590/C567173 |C04.700.645/C567173 |C10.562.600/C567173 |C10.574.500.549/C567173 |C10.597.606.643/C567173 |C16.131.260/C567173 |C16.320.180/C567173 |C16.320.400.560/C567173 |C16.320.700.645/C567173 |C23.550.210.182/C567173 |C23.550.291.812/C56717 |
Synonyms: | |
Slim Mappings: | Cancer|Congenital abnormality|Genetic disease (inborn)|Mental disorder|Nervous system disease|Pathology (process)|Signs and symptoms |
Reference: |
MedGen: C567173
MeSH: C567173
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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