Human Phenotype Ontology 
Grandparent Node:
expandAbnormal heart morphology (HP:0001627)help
Parent Node:
expandAbnormal anatomic location of the heart (HP:0004307)help
..Starting node
..expandMesocardia (HP:0011599)help
Term ID: 11599
Name: Mesocardia
Synonym:
Definition: Mesocardia is an abnormal location of the heart in which the heart is in a midline position and the longitudinal axis of the heart lies in the mid-sagittal plane.
Comments:
Reference: HP:0011599
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal direction of ventricular apex (HP:0011600) help
..expandDextrocardia (HP:0001651) help
..expandEctopia cordis (HP:0001683) 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:0011599HP:0011599Mesocardia0CFC1 CL E G H5599718292OMIM:605376Heterotaxy, visceral, 2, autosomal.13
HP:0011599HP:0011599Mesocardia0MYRF CL E G H7451181OMIM:618280Cardiac-Urogenital syndrome2
HP:0011599HP:0011599Mesocardia0SRCAP CL E G H1084716974ORPHA:2044Floating-Harbor syndromeHP:0040284 - Very rare138
HP:0011599HP:0011599Mesocardia0SRCAP CL E G H1084716974OMIM:136140Floating-Harbor syndromeHP:0040283 - Occasional138


Genes (3) :CFC1 MYRF SRCAP

Diseases (4) :OMIM:605376 OMIM:618280 ORPHA:2044 OMIM:136140
 

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