Human Phenotype Ontology 
Grandparent Node:
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Abnormal delivery (HP:0001787)help
Parent Node:
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Premature birth (HP:0001622)help
Parent Node:
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Premature rupture of membranes (HP:0001788)help
..Starting node
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Premature birth following premature rupture of fetal membranes (HP:0005100)help
Term ID: 5100
Name: Premature birth following premature rupture of fetal membranes
Synonym: Premature birth following premature rupture of foetal membranes
Definition:
Comments:
Reference: HP:0005100
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:0005100HP:0005100Premature birth following premature rupture of fetal membranes0COL5A1 CL E G H12892209OMIM:130000Ehlers-danlos syndrome, type I.660


Genes (1) :COL5A1

Diseases (1) :OMIM:130000
 

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