Transient neonatal hypoglycemia (2p21del)
Symptom Information:
Symptom ID: | OMIM : No Id available | |
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Is a (Whole tree): |
HPO:
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Database Frequency: | 3 / 7739 | |
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All diseases associated with this symptom:
2p21 microdeletion syndrome | (Orphanet:163693) |
Atypical hypotonia - cystinuria syndrome | (Orphanet:238523) |
Hypotonia - cystinuria syndrome | (Orphanet:163690) |