Human Phenotype Ontology 
Grandparent Node:
expandAbnormal oral cavity morphology (HP:0000163)help
Parent Node:
expandAbnormal palate morphology (HP:0000174)help
..Starting node
..expandProminent palatine ridges (HP:0010291)help
Term ID: 10291
Name: Prominent palatine ridges
Synonym: Large lateral palatal folds; Large lateral palatal ridges; Prominent lateral palatal folds; Prominent lateral palatal ridges; Prominent palatine folds
Definition: Increased size and/or number of soft tissue folds on the palatal side of the maxillary alveolar ridge.
Comments:
Reference: HP:0010291
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal hard palate morphology (HP:0100737) help
..expandAbnormal soft palate morphology (HP:0100736) help
..expandHigh palate (HP:0000218) help
..expandNarrow palate (HP:0000189) help
..expandPalatal edema (HP:0031089) help
..expandPalate fistula (HP:0010294) help
..expandPalate telangiectasia (HP:0002707) help
..expandProminent median palatal raphe (HP:0002708) 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:0010291HP:0010291Prominent palatine ridges0ASXL1 CL E G H17102318318ORPHA:97297Bohring-Opitz syndromeHP:0040283 - Occasional145
HP:0010291HP:0010291Prominent palatine ridges0KIF7 CL E G H37465430497OMIM:200990Acrocallosal syndrome167
HP:0010291HP:0010291Prominent palatine ridges0PIGN CL E G H235568967ORPHA:280633Multiple congenital anomalies-hypotonia-seizures syndromeHP:0040282 - Frequent37
HP:0010291HP:0010291Prominent palatine ridges0SIX2 CL E G H1073610888ORPHA:488437SIX2-related frontonasal dysplasiaHP:0040282 - Frequent2


Genes (4) :ASXL1 KIF7 PIGN SIX2

Diseases (4) :ORPHA:97297 OMIM:200990 ORPHA:280633 ORPHA:488437
 

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