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:
Oral cleft (HP:0000202)

Parent Node:
Abnormal lower lip morphology (HP:0000178)

Parent Node:
Cleft lip (HP:0410030)

..Starting node
..Cleft lower lip (HP:0010281)

Term ID:

10281

Name:

Cleft lower lip

Synonym:

Cleft lower lip; Cleft of the lower lip; Lower labial cleft

Definition:

A gap in the lower lip.

Comments:

Reference:

HP:0010281

Genes and Diseases:

Child Nodes:

Sister Nodes:

Cleft upper lip (HP:0000204)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010281	HP:0010281	Cleft lower lip	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.