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 skull morphology (HP:0000929)

Parent Node:
Abnormal sella turcica morphology (HP:0002679)

..Starting node
..Duplication of the sella turcica (HP:0040304)

Term ID:

40304

Name:

Duplication of the sella turcica

Synonym:

Duplicate sella turcica; Duplicated sella turcica

Definition:

Comments:

Reference:

HP:0040304

Genes and Diseases:

Child Nodes:

Sister Nodes:

Deformed sella turcica (HP:0002681)

Large sella turcica (HP:0002690)

Small sella turcica (HP:0010538)

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0040304	HP:0040304	Duplication of the sella turcica	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.