Human Phenotype Ontology 
Grandparent Node:
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Respiratory insufficiency (HP:0002093)help
Parent Node:
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Inspiratory stridor (HP:0005348)help
Parent Node:
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Neonatal respiratory distress (HP:0002643)help
..Starting node
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Neonatal inspiratory stridor (HP:0004875)help
Term ID: 4875
Name: Neonatal inspiratory stridor
Synonym:
Definition:
Comments:
Reference: HP:0004875
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandNeonatal asphyxia (HP:0012768) 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:0004875HP:0004875Neonatal inspiratory stridor0KIF22 CL E G H38356391ORPHA:93360Spondyloepimetaphyseal dysplasia with multiple dislocationsHP:0040283 - Occasional14
HP:0004875HP:0004875Neonatal inspiratory stridor0SCN4A CL E G H632910591ORPHA:684Paramyotonia congenita of Von EulenburgHP:0040282 - Frequent263


Genes (2) :KIF22 SCN4A

Diseases (2) :ORPHA:93360 ORPHA:684
 

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