Abnormality of complement system
Symptom Information:
Symptom ID: | HPO:0005339 | ||
Synonyms: |
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Quality: | |||
Cross references: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the immune system(HPO:0002715) Abnormality of immune system physiology(HPO:0010978) Abnormality of humoral immunity(HPO:0005368) Abnormality of complement system(HPO:0005339) MedDRA: |
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Database Frequency: | 3 / 7739 | ||
Resource: |
All diseases associated with this symptom:
COMPLEMENT COMPONENT C1s DEFICIENCY | (OMIM:613783) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
Partial acquired lipodystrophy | (Orphanet:79087) |