Mild intrauterine growth retardation
Symptom Information:
Symptom ID: | HPO:0008883 | |||
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Growth abnormality(HPO:0001507) Growth delay(HPO:0001510) Intrauterine growth retardation(HPO:0001511) Mild intrauterine growth retardation(HPO:0008883) MedDRA: |
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Database Frequency: | 2 / 7739 | |||
Resource: |
All diseases associated with this symptom:
CHILD syndrome | (Orphanet:139) |
DIAMOND-BLACKFAN ANEMIA 1 | (OMIM:105650) |