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Phenotypic Abnormality (PA): Decreased serum complement factor H

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Root: HP Hierarchy (human phenotype with 3 sub-ontologies PA, MI, ON)

Shortest distance to current term
(+ for parents, - for children)
HP term [HP ID] <#Children> #Domains
(Superfamily|Family)
#Supra-domain
(Single|Duplex|Triple)
+ + + + + + 6:   Phenotypic abnormality [HP:0000118] <25>
+ + + + + 5:   Abnormality of the immune system [HP:0002715] <3>(38|52) (40|29|16)
+ + + + 4:   Abnormality of immune system physiology [HP:0010978] <14>(29|37) (31|22|11)
+ + + 3:   Abnormality of humoral immunity [HP:0005368] <4>(13|15) (13|9|5)
+ + 2:   Abnormality of complement system [HP:0005339] <4>(10|10) (10|7|5)
+ 1:   Complement deficiency [HP:0004431] <8>(6|6) (6|2|1)
0:   Decreased serum complement factor H [HP:0005369] <1>(0|0) (0|0|0)
- 1:   Partial complement factor H deficiency [HP:0008290](0|0) (0|0|0)