Human Phenotype Ontology 
Grandparent Node:
expandAbnormal foot bone ossification (HP:0010675)help
Grandparent Node:
expandAbnormality of the tarsal bones (HP:0001850)help
Parent Node:
expandAbnormal tarsal ossification (HP:0008369)help
..Starting node
..expandDelayed tarsal ossification (HP:0008103)help
Term ID: 8103
Name: Delayed tarsal ossification
Synonym: Delayed ankle bone maturation; Tarsal delayed ossification
Definition: Delayed maturation and calcification of any of the tarsal bones, seven bones of the foot comprising the calcaneus, talus, cuboid, navicular, and the cuneiform bones.
Comments:
Reference: HP:0008103
Genes and Diseases:
 
       Child Nodes:
........expandDelayed calcaneal ossification (HP:0008142) help

 Sister Nodes: 
..expandAdvanced tarsal ossification (HP:0008108) help
..expandDelayed talus ossification (HP:0011836) help
..expandIrregular tarsal ossification (HP:0008134) help
..expandTarsal stippling (HP:0008131) 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:0008103HP:0008103Delayed tarsal ossification0COL2A1 CL E G H12802200OMIM:183900Spondyloepiphyseal dysplasia congenita284
HP:0008103HP:0008103Delayed tarsal ossification0HOXA13 CL E G H32095102OMIM:140000Hand-Foot-Genital syndrome.11
HP:0008103HP:0008103Delayed tarsal ossification0MATN3 CL E G H41486909OMIM:607078Epiphyseal dysplasia, multiple, 5.32
HP:0008103HP:0008103Delayed tarsal ossification0PTH1R CL E G H57459608OMIM:600002Eiken syndrome58
HP:0008103HP:0008142Delayed calcaneal ossification1COL2A1 CL E G H12802200OMIM:183900Spondyloepiphyseal dysplasia congenita.284


Genes (4) :COL2A1 HOXA13 MATN3 PTH1R

Diseases (4) :OMIM:183900 OMIM:140000 OMIM:607078 OMIM:600002
 

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