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Term ID: | 5596 |
Name: | Hypoparathyroidism, X-Linked |
Definition: | |
Alternative IDs: | OMIM:307700 |
ParentIDs: | MESH:D007011|MESH:D040181 |
TreeNumbers: | C16.320.322/C562782 |C19.642.482/C562782 |
Synonyms: | HYPX |PARATHYROID GLANDS, AGENESIS OF |
Slim Mappings: | Endocrine system disease|Genetic disease (inborn) |
Reference: |
MedGen: C562782
MeSH: C562782
OMIM: 307700;
Genes: HPT; | Phenotypes | | Disease Causing ClinVar Variants | |
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