Human Phenotype Ontology 
Grandparent Node:
expand
Inability to walk (HP:0002540)help
Parent Node:
expand
Progressive inability to walk (HP:0002505)help
..Starting node
..expand
Loss of ability to walk in first decade (HP:0006794)help
Term ID: 6794
Name: Loss of ability to walk in first decade
Synonym: Loss of ability to walk in first decade
Definition:
Comments:
Reference: HP:0006794
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandInability to walk by childhood/adolescence (HP:0006915) help
..expandLoss of ability to walk (HP:0006957) help
InputHPO IDHPO termDistanceGeneGene id entrezDiseaseIdDiseaseNameDiseaseMIMConceptIDSourceTypical associationHGMD variantsClinVar variantsHGNC IDGeneMIM
 
HPO disease - gene - phenotype typical associations:
HP:0006794HP:0006794Loss of ability to walk in first decade0MYOT CL E G H949998911ORPHA11618812399604103
HP:0006794HP:0006794Loss of ability to walk in first decade0SLC9A6 CL E G H10479300243Christianson syndrome300243C2678194OMIM12835111079300231
 
HPO disease - gene - phenotype less frequent non-typical associations:


Genes (2) :MYOT SLC9A6

Diseases (2) :98911 300243
 

Human Phenotype Ontology(HPO) is developed by the Human Phenotype Ontology Consortium. The version used here is June 2019 release.