Human Phenotype Ontology 
Grandparent Node:
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Abnormal nasopharynx morphology (HP:0001739)help
Grandparent Node:
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Abnormality of the tonsils (HP:0100765)help
Parent Node:
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Abnormal nasopharyngeal adenoid morphology (HP:3000033)help
..Starting node
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Abnormal size of nasopharyngeal adenoids (HP:0040257)help
Term ID: 40257
Name: Abnormal size of nasopharyngeal adenoids
Synonym:
Definition: A deviation in the size of nasopharyngeal adenoids.
Comments:
Reference: HP:0040257
Genes and Diseases:
 
       Child Nodes:
........expandDecreased size of nasopharyngeal adenoids (HP:0040260) help
................... HP:0040258 Hypoplastic nasopharyngeal adenoids
........expandIncreased size of nasopharyngeal adenoids (HP:0040261) help

 Sister Nodes: 
..expandAdenoiditis (HP:0031458) help
..expandAplastic/Hypoplastic nasopharyngeal adenoids (HP:0040256) help
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0040257HP:0040257Abnormal size of nasopharyngeal adenoids0IDS CL E G H34235389ORPHA:217093Mucopolysaccharidosis type 2, attenuated form86
HP:0040257HP:0040257Abnormal size of nasopharyngeal adenoids0IDS CL E G H34235389ORPHA:217085Mucopolysaccharidosis type 2, severe form86
HP:0040257HP:0040257Abnormal size of nasopharyngeal adenoids0RSPRY1 CL E G H8997029420ORPHA:457395Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndrome2
HP:0040257HP:0040257Abnormal size of nasopharyngeal adenoids0ZBTB7A CL E G H5134118078OMIM:619769MACROCEPHALY, NEURODEVELOPMENTAL DELAY, LYMPHOID HYPERPLASIA, AND PERSISTENT FETAL HEMOGLOBIN; MNDLFH
HP:0040257HP:0040260Decreased size of nasopharyngeal adenoids1 CL E G H
HP:0040257HP:0040261Increased size of nasopharyngeal adenoids1IDS CL E G H34235389ORPHA:217093Mucopolysaccharidosis type 2, attenuated formHP:0040282 - Frequent86
HP:0040257HP:0040261Increased size of nasopharyngeal adenoids1IDS CL E G H34235389ORPHA:217085Mucopolysaccharidosis type 2, severe formHP:0040282 - Frequent86
HP:0040257HP:0040261Increased size of nasopharyngeal adenoids1RSPRY1 CL E G H8997029420ORPHA:457395Progressive spondyloepimetaphyseal dysplasia-short stature-short fourth metatarsals-intellectual disability syndromeHP:0040282 - Frequent2
HP:0040257HP:0040261Increased size of nasopharyngeal adenoids1ZBTB7A CL E G H5134118078OMIM:619769MACROCEPHALY, NEURODEVELOPMENTAL DELAY, LYMPHOID HYPERPLASIA, AND PERSISTENT FETAL HEMOGLOBIN; MNDLFH
HP:0040257HP:0040258Hypoplastic nasopharyngeal adenoids2 CL E G H


Genes (3) :IDS RSPRY1 ZBTB7A

Diseases (4) :ORPHA:217093 ORPHA:217085 ORPHA:457395 OMIM:619769
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is December 15 2022 release.