Human Phenotype Ontology 
Grandparent Node:
expandAbnormal sacrum morphology (HP:0005107)help
Grandparent Node:
expandVertebral segmentation defect (HP:0003422)help
Parent Node:
expandSacral segmentation defect (HP:0008490)help
..Starting node
..expandHemisacrum (HP:0009790)help
Term ID: 9790
Name: Hemisacrum
Synonym:
Definition: A hemisacral defect involving the sacral vertebrae S2 to S5. In hemisacrum, the first sacral vertebra is intact and there is agenesis involving only S2-S5.
Comments:
Reference: HP:0009790
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal sacral segmentation (HP:0008468) help
..expandBifid sacrum (HP:0009791) 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:0009790HP:0009790Hemisacrum0MNX1 CL E G H31104979OMIM:176450Currarino syndrome17
HP:0009790HP:0009790Hemisacrum0VANGL1 CL E G H8183915512OMIM:600145Sacral defect with anterior meningocele.111


Genes (2) :MNX1 VANGL1

Diseases (2) :OMIM:176450 OMIM:600145
 

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