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:
Abnormality of the mouth (HP:0000153)

Parent Node:
Abnormal head blood vessel morphology (HP:3000036)

Parent Node:
Abnormal oral morphology (HP:0031816)

..Starting node
..Abnormal inferior alveolar artery morphology (HP:3000054)

Term ID:

3000054

Name:

Abnormal inferior alveolar artery morphology

Synonym:

Definition:

An abnormality of an inferior alveolar artery.

Comments:

Reference:

HP:3000054

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormal mandible condylar process morphology (HP:3000077)

Abnormal mandible coronoid process morphology (HP:3000078)

Abnormal oral cavity morphology (HP:0000163)

Oral cleft (HP:0000202)

Pierre-Robin sequence (HP:0000201)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:3000054	HP:3000054	Abnormal inferior alveolar artery morphology	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.