Human Phenotype Ontology 
Grandparent Node:
expandAbnormal palate morphology (HP:0000174)help
Parent Node:
expandAbnormal hard palate morphology (HP:0100737)help
..Starting node
..expandShort hard palate (HP:0010290)help
Term ID: 10290
Name: Short hard palate
Synonym: Decreased length of hard palate; Hypoplastic palate; Short palate
Definition: Distance between the labial point of the incisive papilla to the midline junction of the hard and soft palate more than 2 SD below the mean (objective) or apparently decreased length of the hard palate (subjective).
Comments:
Reference: HP:0010290
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandCleft palate (HP:0000175) help
..expandTorus palatinus (HP:0100789) 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:0010290HP:0010290Short hard palate0DVL1 CL E G H18553084OMIM:180700Robinow syndrome, autosomal dominant 1.14
HP:0010290HP:0010290Short hard palate0GLI2 CL E G H27364318OMIM:610829Holoprosencephaly 9173
HP:0010290HP:0010290Short hard palate0SNRPB CL E G H662811153ORPHA:1393Cerebrocostomandibular syndromeHP:0040283 - Occasional6
HP:0010290HP:0010290Short hard palate0SNRPB CL E G H662811153OMIM:117650Cerebrocostomandibular syndrome.6
HP:0010290HP:0010290Short hard palate0WNT5A CL E G H747412784OMIM:180700Robinow syndrome, autosomal dominant 1.98


Genes (4) :DVL1 GLI2 SNRPB WNT5A

Diseases (4) :OMIM:180700 OMIM:610829 ORPHA:1393 OMIM:117650
 

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