Human Phenotype Ontology 
Grandparent Node:
expandAbnormal pelvic girdle bone morphology (HP:0002644)help
Grandparent Node:
expandLimitation of joint mobility (HP:0001376)help
Parent Node:
expandLimited hip movement (HP:0008800)help
..Starting node
..expandLimited hip extension (HP:0003093)help
Term ID: 3093
Name: Limited hip extension
Synonym: Limited hip extension; Restricted hip extension
Definition: Limitation of the extension of the hip, i.e., decreased ability to straighten the hip joint and thereby increase the angle between torso and thigh; moving the thigh or top of the pelvis backward.
Comments:
Reference: HP:0003093
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandDecreased hip abduction (HP:0003184) help
..expandHip contracture (HP:0003273) 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:0003093HP:0003093Limited hip extension0CHST3 CL E G H94691971OMIM:143095Spondyloepiphyseal dysplasia with congenital joint dislocations.165
HP:0003093HP:0003093Limited hip extension0COMP CL E G H13112227OMIM:177170Pseudoachondroplasia89
HP:0003093HP:0003093Limited hip extension0COMP CL E G H13112227ORPHA:750PseudoachondroplasiaHP:0040283 - Occasional89
HP:0003093HP:0003093Limited hip extension0DST CL E G H6671090OMIM:614653Neuropathy, hereditary sensory and autonomic, type VI.108
HP:0003093HP:0003093Limited hip extension0FGFR3 CL E G H22613690OMIM:100800ACHONDROPLASIA.145
HP:0003093HP:0003093Limited hip extension0KY CL E G H33985526576OMIM:617114MYOPATHY, MYOFIBRILLAR, 7; MFM73


Genes (5) :CHST3 COMP DST FGFR3 KY

Diseases (6) :OMIM:143095 OMIM:177170 ORPHA:750 OMIM:614653 OMIM:100800 OMIM:617114
 

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