Human Phenotype Ontology

Hello! Guest! Please Login or Register! Clinician Mode

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 helix morphology (HP:0011039)

Parent Node:
Abnormal incisura morphology (HP:0031228)

..Starting node
..Decreased incisura length (HP:0031230)

Term ID:

31230

Name:

Decreased incisura length

Synonym:

Definition:

The length of the incisura from the upper to lower border is less than that observed in the average population.

Comments:

Reference:

HP:0031230

Genes and Diseases:

Child Nodes:

Sister Nodes:

Increased incisura length (HP:0031229)

Increased incisura width (HP:0031232)

Narrow incisura width (HP:0031231)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0031230	HP:0031230	Decreased incisura length	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.