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 facial skeleton morphology (HP:0011821)

Parent Node:
Abnormal midface morphology (HP:0000309)

Parent Node:
Abnormal zygomatic bone morphology (HP:0010668)

..Starting node
..obsolete Abnormal malar bone morphology (HP:0012369)

Term ID:

12369

Name:

obsolete Abnormal malar bone morphology

Synonym:

Definition:

Comments:

Reference:

HP:0012369

Genes and Diseases:

Child Nodes:

........

Malar flattening (HP:0000272)

........

Malar prominence (HP:0010620)

Sister Nodes:

Abnormal zygomatic arch morphology (HP:0005557)

Hypoplasia of the zygomatic bone (HP:0010669)

Prominence of the zygomatic bone (HP:0012370)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0012369	HP:0012369	obsolete Abnormal malar bone 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.