Human Phenotype Ontology 
Grandparent Node:
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Abnormal thorax morphology (HP:0000765)help
Parent Node:
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Thoracic hypoplasia (HP:0005257)help
..Starting node
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Congenital microthorax (HP:0006647)help
Term ID: 6647
Name: Congenital microthorax
Synonym:
Definition:
Comments:
Reference: HP:0006647
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandNarrow chest (HP:0000774) help
..expandUnilateral chest hypoplasia (HP:0005254) 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:0006647HP:0006647Congenital microthorax0 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.