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 facial skeleton morphology (HP:0011821)

Parent Node:
Abnormal paranasal sinus morphology (HP:0000245)

..Starting node
..Advanced pneumatization of cranial sinuses (HP:0010540)

Term ID:

10540

Name:

Advanced pneumatization of cranial sinuses

Synonym:

Definition:

A degree of pneumatization that is increased compared to age-related norms.

Comments:

Reference:

HP:0010540

Genes and Diseases:

Child Nodes:

Sister Nodes:

Abnormality of ethmoid sinus (HP:3000040)

Abnormality of frontal sinus (HP:0002687)

Abnormality of the maxillary sinus (HP:0430023)

Abnormality of the sphenoid sinus (HP:0430022)

Aplasia/Hypoplasia involving the sinuses (HP:0009120)

Paranasal sinus neoplasm (HP:0030072)

Sinusitis (HP:0000246)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0010540	HP:0010540	Advanced pneumatization of cranial sinuses	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.