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:
Abnormal intestine morphology (HP:0002242)

Grandparent Node:
Gastrointestinal hemorrhage (HP:0002239)

Parent Node:
Abnormality of the small intestine (HP:0002244)

Parent Node:
Intestinal bleeding (HP:0002584)

..Starting node
..Small intestinal bleeding (HP:0012849)

Term ID:

12849

Name:

Small intestinal bleeding

Synonym:

Small intestinal bleeding; Small intestinal haemorrhage; Small intestinal hemorrhage

Definition:

Bleeding from the small intestine.

Comments:

Reference:

HP:0012849

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012849	HP:0012849	Small intestinal bleeding	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.