Human Phenotype Ontology 
Grandparent Node:
expandAbnormal rib cage morphology (HP:0001547)help
Parent Node:
expandAbnormal rib morphology (HP:0000772)help
..Starting node
..expandAnomalous rib insertion to vertebrae (HP:0006593)help
Term ID: 6593
Name: Anomalous rib insertion to vertebrae
Synonym:
Definition:
Comments:
Reference: HP:0006593
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal rib ossification (HP:0012306) help
..expandAbnormality of the costochondral junction (HP:0000919) help
..expandAplasia/Hypoplasia of the ribs (HP:0006712) help
..expandBeaded ribs (HP:0000923) help
..expandBifid ribs (HP:0000892) help
..expandBroad ribs (HP:0000885) help
..expandCalcification of ribs (HP:0040059) help
..expandCoat hanger sign of ribs (HP:0006665) help
..expandCupped ribs (HP:0000887) help
..expandFlaring of rib cage (HP:0000904) help
..expandHorizontal ribs (HP:0000888) help
..expandMultiple rib fractures (HP:0006640) help
..expandProminent floating ribs (HP:0006641) help
..expandRib exostoses (HP:0000896) help
..expandRib fusion (HP:0000902) help
..expandRib gap (HP:0030280) help
..expandRib segmentation abnormalities (HP:0006655) help
..expandSuperior rib anomalies (HP:0005820) help
..expandSupernumerary ribs (HP:0005815) help
..expandThickened ribs (HP:0000900) help
..expandThin ribs (HP:0000883) help
..expandUndulate ribs (HP:0010561) 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:0006593HP:0006593Anomalous rib insertion to vertebrae0SNRPB CL E G H662811153OMIM:117650Cerebrocostomandibular syndrome.6


Genes (1) :SNRPB

Diseases (1) :OMIM:117650
 

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