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Term ID: | 2333 |
Name: | CHROMOSOME 7q11.23 DELETION SYNDROME, DISTAL, 1.2-MB |
Definition: | |
Alternative IDs: | |
ParentIDs: | MESH:D002872|MESH:D004827|MESH:D007859|MESH:D008607 |
TreeNumbers: | C10.228.140.490/613729 |C10.597.606.150.550/613729 |C10.597.606.643/613729 |C23.550.210.050.500.500/613729 |C23.888.592.604.150.550/613729 |C23.888.592.604.646/613729 |F03.550.350.500/613729 |F03.550.450/613729 |F03.550.600/613729 |
Synonyms: | DISTAL CHROMOSOME 7q11.23 DELETION SYNDROME |
Slim Mappings: | Mental disorder|Nervous system disease|Pathology (process)|Signs and symptoms |
Reference: |
MedGen: 613729
MeSH: 613729
OMIM: 613729;
Genes: AF8T; | Phenotypes | | Disease Causing ClinVar Variants | |
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