Human Phenotype Ontology 
Grandparent Node:
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Pneumothorax (HP:0002107)help
Parent Node:
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Spontaneous pneumothorax (HP:0002108)help
..Starting node
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Spontaneous neonatal pneumothorax (HP:0004876)help
Term ID: 4876
Name: Spontaneous neonatal pneumothorax
Synonym: Neonatal pneumothorax
Definition: Pneumothorax occurring neonatally without traumatic injury to the chest or lung.
Comments:
Reference: HP:0004876
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
InputHPO IDHPO termDistanceGeneGene id entrezHGNC IDDiseaseIdDiseaseNameFrequencyOnsetHGMD variantsClinVar variants
 
HPO disease - gene - phenotype typical associations:
 
HPO disease - gene - phenotype less frequent non-typical associations:
HP:0004876HP:0004876Spontaneous neonatal pneumothorax0ADAMTS2 CL E G H9509218OMIM:225410Ehlers-Danlos syndrome, type VII, autosomal recessive.165
HP:0004876HP:0004876Spontaneous neonatal pneumothorax0SFTPB CL E G H643910801ORPHA:217563Neonatal acute respiratory distress due to SP-B deficiencyHP:0040283 - Occasional51


Genes (2) :ADAMTS2 SFTPB

Diseases (2) :OMIM:225410 ORPHA:217563
 

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