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:
Abdominal symptom (HP:0011458)

Parent Node:
Abnormal bowel sounds (HP:0030142)

..Starting node
..Hypoactive bowel sounds (HP:0030144)

Term ID:

30144

Name:

Hypoactive bowel sounds

Synonym:

Decreased bowel sounds

Definition:

An decreased amount of bowel sounds.

Comments:

Reference:

HP:0030144

Genes and Diseases:

Child Nodes:

Sister Nodes:

Hyperactive bowel sounds (HP:0030143)

Lack of bowel sounds (HP:0030145)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0030144	HP:0030144	Hypoactive bowel sounds	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.