Human Phenotype Ontology 
Grandparent Node:
expandAbnormalities of placenta or umbilical cord (HP:0001194)help
Parent Node:
expandAbnormality of the umbilical cord (HP:0010881)help
..Starting node
..expandAbnormal insertion of umbilical cord (HP:0011418)help
Term ID: 11418
Name: Abnormal insertion of umbilical cord
Synonym:
Definition: Anomalous location of the insertion of umbilical cord in the placenta. Normally, the insertion is at least two centimers distant from the edge of the placenta.
Comments:
Reference: HP:0011418
Genes and Diseases:
 
       Child Nodes:
........expandMarginal umbilical cord insertion (HP:0030658) help
........expandVelamentous cord insertion (HP:0030659) help
........expandFurcate cord insertion (HP:0030660) help

 Sister Nodes: 
..expandAbnormal umbilical cord blood vessel morphology (HP:0011403) help
..expandLong umbilical cord (HP:0011417) help
..expandShort umbilical cord (HP:0001196) help
..expandUmbilical cord cyst (HP:0030654) help
..expandUmbilical cord hematoma (HP:0030657) help
..expandUmbilical cord knot (HP:0030655) help
..expandUmbilical vein varix (HP:0030656) 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:0011418HP:0011418Abnormal insertion of umbilical cord0 CL E G H
HP:0011418HP:0030660Furcate cord insertion1 CL E G H
HP:0011418HP:0030659Velamentous cord insertion1 CL E G H
HP:0011418HP:0030658Marginal umbilical cord insertion1 CL E G H
HP:0011418HP:0033991Vasa previa1 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.