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:
Diarrhea (HP:0002014)

Parent Node:
Bloody diarrhea (HP:0025085)

..Starting node
..Bloody mucoid diarrhea (HP:0025086)

Term ID:

25086

Name:

Bloody mucoid diarrhea

Synonym:

Bloody mucoid diarrhoea

Definition:

Passage of many stools containing blood and mucus.

Comments:

Reference:

HP:0025086

Genes and Diseases:

Child Nodes:

Sister Nodes:

Hematochezia (HP:0002573)

Melena (HP:0002249)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025086	HP:0025086	Bloody mucoid diarrhea	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.