Human Phenotype Ontology 
Grandparent Node:
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Abnormal left ventricle morphology (HP:0001711)help
Parent Node:
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Morphological abnormality of the papillary muscles (HP:0025445)help
..Starting node
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Anomalous insertion of papillary muscle directly into anterior mitral leaflet (HP:0025446)help
Term ID: 25446
Name: Anomalous insertion of papillary muscle directly into anterior mitral leaflet
Synonym:
Definition: A congenital malformation in which one or both of the papillary muscles (posteromedial or anterolateral) insert directly (that is, without interpositioned chordae tendineae) into the anterior mitral leaflet.
Comments:
Reference: HP:0025446
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandDisplacement of the papillary muscles (HP:0025447) 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:0025446HP:0025446Anomalous insertion of papillary muscle directly into anterior mitral leaflet0 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.