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Term ID: | 8135 |
Name: | N syndrome |
Definition: | |
Alternative IDs: | OMIM:310465 |
ParentIDs: | MESH:D008607|MESH:D015458|MESH:D049914 |
TreeNumbers: | C04.557.337.428.580/C536108 |C10.597.606.643/C536108 |C15.604.515.560.575/C536108 |C18.452.284/C536108 |C20.683.515.528.582/C536108 |C23.888.592.604.646/C536108 |F03.550.600/C536108 |
Synonyms: | NSX |
Slim Mappings: | Cancer|Immune system disease|Lymphatic disease|Mental disorder|Metabolic disease|Nervous system disease|Signs and symptoms |
Reference: |
MedGen: C536108
MeSH: C536108
OMIM: 310465;
Genes: POLA1; | Phenotypes | | Disease Causing ClinVar Variants | |
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