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Term ID: | 8050 |
Name: | NF1 Microdeletion Syndrome |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D002872|MESH:D007859|MESH:D008607|MESH:D017253|MESH:D019465 |
TreeNumbers: | C04.557.580.600.580.590/C563524 |C04.700.645/C563524 |C05.660.207/C563524 |C10.562.600/C563524 |C10.574.500.549/C563524 |C10.597.606.150.550/C563524 |C10.597.606.643/C563524 |C16.131.621.207/C563524 |C16.320.400.560/C563524 |C16.320.700.645/C563524 |C23.550.210.05 |
Synonyms: | |
Slim Mappings: | Cancer|Congenital abnormality|Genetic disease (inborn)|Mental disorder|Musculoskeletal disease|Nervous system disease|Pathology (process)|Signs and symptoms |
Reference: |
MedGen: C563524
MeSH: C563524
OMIM:
Genes: | Phenotypes | | Disease Causing ClinVar Variants | |
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