Human Phenotype Ontology 
Grandparent Node:
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Abnormality of bone mineral density (HP:0004348)help
Parent Node:
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Abnormal scapula morphology (HP:0000782)help
Parent Node:
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Increased bone mineral density (HP:0011001)help
..Starting node
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Sclerotic scapulae (HP:0001474)help
Term ID: 1474
Name: Sclerotic scapulae
Synonym:
Definition: Increased density of the bony tissue of the scapula.
Comments:
Reference: HP:0001474
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandBone-in-a-bone appearance of carpal bones (HP:0004234) help
..expandClavicular sclerosis (HP:0100923) help
..expandCortical sclerosis (HP:0005652) help
..expandCraniofacial osteosclerosis (HP:0005464) help
..expandGeneralized osteosclerosis (HP:0005789) help
..expandIncreased bone density with cystic changes (HP:0005700) help
..expandIncreased density of long bones (HP:0006392) help
..expandIncreased skull ossification (HP:0004330) help
..expandIvory epiphyses of the metacarpals (HP:0009191) help
..expandMetacarpal diaphyseal endosteal sclerosis (HP:0006174) help
..expandOsteopetrosis (HP:0011002) help
..expandOsteopoikilosis (HP:0010739) help
..expandPatchy osteosclerosis (HP:0005686) help
..expandSclerosis of foot bone (HP:0100925) help
..expandSclerosis of hand bone (HP:0004054) help
..expandSclerosis of skull base (HP:0002694) 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:0001474HP:0001474Sclerotic scapulae0LEMD3 CL E G H2359228887ORPHA:166119Isolated osteopoikilosis68
HP:0001474HP:0001474Sclerotic scapulae0SOST CL E G H5096413771OMIM:269500Sclerosteosis 1.26


Genes (2) :LEMD3 SOST

Diseases (2) :ORPHA:166119 OMIM:269500
 

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