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

..Starting node
..Type 1 congenital pulmonary airway malformation (HP:0025725)

Term ID:

25725

Name:

Type 1 congenital pulmonary airway malformation

Synonym:

Definition:

A type of congenital pulmonary airway malformation that is characterized by multiple large cysts or a single dominant cyst.

Comments:

Reference:

HP:0025725

Genes and Diseases:

Child Nodes:

Sister Nodes:

Input	HPO ID	HPO term	Distance	Gene
HPO disease - gene - phenotype typical associations:
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0025725	HP:0025725	Type 1 congenital pulmonary airway malformation	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.