Human Phenotype Ontology 
Grandparent Node:
expandAbnormal rib cage morphology (HP:0001547)help
Parent Node:
expandAbnormal rib morphology (HP:0000772)help
..Starting node
..expandCoat hanger sign of ribs (HP:0006665)help
Term ID: 6665
Name: Coat hanger sign of ribs
Synonym: Coat hanger sign of ribs
Definition: An abnormal morphology of the ribs consisting of shorted, abnormally curved ribs. On posteroanterior chest radiography, the ribs show a curvature resembling that of a coat hanger (clothes hanger).
Comments:
Reference: HP:0006665
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal rib ossification (HP:0012306) help
..expandAbnormality of the costochondral junction (HP:0000919) help
..expandAnomalous rib insertion to vertebrae (HP:0006593) 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
..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:0006665HP:0006665Coat hanger sign of ribs0DLK1 CL E G H87882907ORPHA:254534Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylationHP:0040281 - Very frequent1
HP:0006665HP:0006665Coat hanger sign of ribs0DLK1 CL E G H87882907ORPHA:254528Kagami-Ogata syndrome due to maternal 14q32.2 microdeletionHP:0040281 - Very frequent1
HP:0006665HP:0006665Coat hanger sign of ribs0DLK1 CL E G H87882907ORPHA:96334Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14HP:0040280 - Obligate1
HP:0006665HP:0006665Coat hanger sign of ribs0FLNA CL E G H23163754OMIM:305620Frontometaphyseal dysplasia.493
HP:0006665HP:0006665Coat hanger sign of ribs0MEG3 CL E G H5538414575ORPHA:254534Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylationHP:0040281 - Very frequent1
HP:0006665HP:0006665Coat hanger sign of ribs0MEG3 CL E G H5538414575ORPHA:254528Kagami-Ogata syndrome due to maternal 14q32.2 microdeletionHP:0040281 - Very frequent1
HP:0006665HP:0006665Coat hanger sign of ribs0MEG3 CL E G H5538414575ORPHA:96334Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14HP:0040280 - Obligate1
HP:0006665HP:0006665Coat hanger sign of ribs0RTL1 CL E G H38801514665ORPHA:254534Kagami-Ogata syndrome due to maternal 14q32.2 hypermethylationHP:0040281 - Very frequent
HP:0006665HP:0006665Coat hanger sign of ribs0RTL1 CL E G H38801514665ORPHA:254528Kagami-Ogata syndrome due to maternal 14q32.2 microdeletionHP:0040281 - Very frequent
HP:0006665HP:0006665Coat hanger sign of ribs0RTL1 CL E G H38801514665ORPHA:96334Kagami-Ogata syndrome due to paternal uniparental disomy of chromosome 14HP:0040280 - Obligate


Genes (4) :DLK1 FLNA MEG3 RTL1

Diseases (4) :ORPHA:254534 ORPHA:254528 ORPHA:96334 OMIM:305620
 

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