Human Phenotype Ontology 
Grandparent Node:
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Abnormality of immune system physiology (HP:0010978)help
Parent Node:
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Sepsis (HP:0100806)help
..Starting node
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Neonatal sepsis (HP:0040187)help
Term ID: 40187
Name: Neonatal sepsis
Synonym:
Definition: Systemic inflammatory response to infection in newborn babies.
Comments:
Reference: HP:0040187
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:0040187HP:0040187Neonatal sepsis0COG4 CL E G H2583918620ORPHA:263501COG4-CDGHP:0040283 - Occasional67
HP:0040187HP:0040187Neonatal sepsis0G6PC3 CL E G H9257924861OMIM:612541Neutropenia, severe congenital, 4, autosomal recessive37
HP:0040187HP:0040187Neonatal sepsis0IL7R CL E G H35756024ORPHA:169154T-B+ severe combined immunodeficiency due to IL-7Ralpha deficiencyHP:0040283 - Occasional94
HP:0040187HP:0040187Neonatal sepsis0SERAC1 CL E G H8494721061OMIM:6147393-Methylglutaconic aciduria with deafness, encephalopathy, and leigh-like syndrome.47


Genes (4) :COG4 G6PC3 IL7R SERAC1

Diseases (4) :ORPHA:263501 OMIM:612541 ORPHA:169154 OMIM:614739
 

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