Birth weight <2,500gm
Symptom Information:
Symptom ID: | OMIM : No Id available | ||
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
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Database Frequency: | 2 / 7739 | ||
Resource: |
All diseases associated with this symptom:
Autosomal recessive Kenny-Caffey syndrome | (Orphanet:93324) |
Smith-Lemli-Opitz syndrome | (Orphanet:818) |