Human Phenotype Ontology 
Grandparent Node:
expandobsolete Abnormal morphology of bones of the lower limbs (HP:0040066)help
Parent Node:
expandAbnormality of femur morphology (HP:0002823)help
..Starting node
..expandDisproportionate prominence of the femoral medial condyle (HP:0006437)help
Term ID: 6437
Name: Disproportionate prominence of the femoral medial condyle
Synonym:
Definition:
Comments:
Reference: HP:0006437
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandAbnormal femoral metaphysis morphology (HP:0006489) help
..expandAbnormal femoral neck/head morphology (HP:0003366) help
..expandAbnormal femoral torsion (HP:0031069) help
..expandAbnormality of femoral epiphysis (HP:0006499) help
..expandAplasia/hypoplasia of the femur (HP:0005613) help
..expandBifid femur (HP:0010443) help
..expandClub-shaped distal femur (HP:0006384) help
..expandClub-shaped proximal femur (HP:0006406) help
..expandDistal tapering femur (HP:0006408) help
..expandDumbbell-shaped femur (HP:0006375) help
..expandErlenmeyer flask deformity of the femurs (HP:0004975) help
..expandFemoral bowing (HP:0002980) help
..expandFemoral spur (HP:0031171) help
..expandFemur fracture (HP:0031846) help
..expandIncreased femoral anteversion (HP:0012427) help
..expandLow femoral bone density (HP:0031163) help
..expandTrapezoidal distal femoral condyles (HP:0006432) 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:0006437HP:0006437Disproportionate prominence of the femoral medial condyle0LMX1B CL E G H40106654OMIM:161200Nail-Patella syndrome.165


Genes (1) :LMX1B

Diseases (1) :OMIM:161200
 

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