Human Phenotype Ontology 
Grandparent Node:
expandAbnormality of the abdominal organs (HP:0002012)help
Grandparent Node:
expandHeterotaxy (HP:0030853)help
Parent Node:
expandAbnormality of abdominal situs (HP:0011620)help
..Starting node
..expandAbdominal situs ambiguus (HP:0031565)help
Term ID: 31565
Name: Abdominal situs ambiguus
Synonym:
Definition: An abnormality in which the abdominal organs are positioned in such a way with respect to each other and the left-right axis as to be not clearly lateralised and thus have neither the usual, or normal (situs solitus), nor the mirror-imaged (situs inversus) arrangements.
Comments:
Reference: HP:0031565
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbdominal situs inversus (HP:0003363) 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:0031565HP:0031565Abdominal situs ambiguus0CIROP CL E G H10012890853647OMIM:619702HETEROTAXY, VISCERAL, 12, AUTOSOMAL; HTX12
HP:0031565HP:0031565Abdominal situs ambiguus0GDF1 CL E G H26574214OMIM:208530Right atrial isomerism (Ivemark)28
HP:0031565HP:0031565Abdominal situs ambiguus0NODAL CL E G H48387865OMIM:270100Heterotaxy, visceral, 545


Genes (3) :CIROP GDF1 NODAL

Diseases (3) :OMIM:619702 OMIM:208530 OMIM:270100
 

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