Complement deficiency
Symptom Information:
Symptom ID: | HPO:0004431 | ||||||
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) Complement deficiency(HPO:0004431) MedDRA: |
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Database Frequency: | 10 / 7739 | ||||||
Resource: |
All diseases associated with this symptom:
COMPLEMENT COMPONENT 4A DEFICIENCY | (OMIM:614380) |
COMPLEMENT COMPONENT 6 DEFICIENCY | (OMIM:612446) |
COMPLEMENT COMPONENT 7 DEFICIENCY | (OMIM:610102) |
COMPLEMENT COMPONENT C1r/C1s DEFICIENCY | (OMIM:216950) |
Familial partial lipodystrophy, Dunnigan type | (Orphanet:2348) |
Hypocomplementemic urticarial vasculitis | (Orphanet:36412) |
Immunodeficiency due to a late component of complements deficiency | (Orphanet:169150) |
MASP2 DEFICIENCY | (OMIM:613791) |
Partial acquired lipodystrophy | (Orphanet:79087) |
Recurrent Neisseria infections due to factor D deficiency | (Orphanet:169467) |