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 size of nasopharyngeal adenoids (HP:0040257)

Parent Node:
Aplastic/Hypoplastic nasopharyngeal adenoids (HP:0040256)

Parent Node:
Decreased size of nasopharyngeal adenoids (HP:0040260)

..Starting node
..Hypoplastic nasopharyngeal adenoids (HP:0040258)

Term ID:

40258

Name:

Hypoplastic nasopharyngeal adenoids

Synonym:

Underdeveloped nasopharyngeal adenoids

Definition:

Underdevelopment of the nasopharyngeal adenoids.

Comments:

Reference:

HP:0040258

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:0040258	HP:0040258	Hypoplastic nasopharyngeal adenoids	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.