Isolated growth hormone deficiency
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Is a (Whole tree): |
HPO:
MedDRA: |
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Database Frequency: | 4 / 7739 | |
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All diseases associated with this symptom:
Isolated growth hormone deficiency type IA | (Orphanet:231662) |
Isolated growth hormone deficiency type II | (Orphanet:231679) |
Microform holoprosencephaly | (Orphanet:280200) |
Solitary median maxillary central incisor syndrome | (Orphanet:2286) |