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

Grandparent Node:
Phenotypic abnormality (HP:0000118)

Parent Node:
Abnormal cellular phenotype (HP:0025354)

..Starting node
..obsolete Abnormal cellular physiology (HP:0025462)

Term ID:

25462

Name:

obsolete Abnormal cellular physiology

Synonym:

Definition:

Comments:

Reference:

HP:0025462

Genes and Diseases:

Child Nodes:

........

Abnormality of redox activity (HP:0025463)

................... HP:0025464 Increased reactive oxygen species production

........

Abnormal cell proliferation (HP:0031377)

................... HP:0031378 Abnormal lymphocyte proliferation

Sister Nodes:

Abnormal cell morphology (HP:0025461)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025462	HP:0025462	obsolete Abnormal cellular physiology	0	CL E G H

Genes (0) :

Diseases (0) :

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