Normal parathyroid hormone
Symptom Information:
Symptom ID: | OMIM : No Id available | ||
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 2 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal dominant primary hypomagnesemia with hypocalcuria | (Orphanet:34528) |
Intellectual deficit, X-linked - craniofacioskeletal syndrome | (Orphanet:163979) |