Human Phenotype Ontology

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Examples Gene: MT-ND1, POLG, Region: M:1-1000 Variant: m.8993T>G, 1:g.10042757T>C rs3888511 MSCV_0000006, ClinVar: RCV000000015, Disease: Leigh syndrome, Phenotype: Retinopathy

..Starting node
..Decreased serum complement C7 (HP:0033058)

Term ID:

33058

Name:

Decreased serum complement C7

Synonym:

Definition:

A reduced level of the complement component C7 in the blood circulation.

Comments:

Reference:

HP:0033058

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene	Gene id entrez	HGNC ID	DiseaseId	DiseaseName	ClinVar variants
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0033058	HP:0033058	Decreased serum complement C7	0	C7 CL E G H	730	1346	OMIM:610102	COMPLEMENT COMPONENT 7 DEFICIENCY; C7D	14

Genes (1) :C7

Diseases (1) :OMIM:610102

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.