Human Phenotype Ontology 
Grandparent Node:
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Osteoporosis (HP:0000939)help
Parent Node:
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Generalized osteoporosis (HP:0040160)help
..Starting node
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Severe generalized osteoporosis (HP:0005897)help
Term ID: 5897
Name: Severe generalized osteoporosis
Synonym: Severe generalised osteoporosis; Severe, generalised osteoporosis; Severe, generalized osteoporosis
Definition: Severe degree of osteoporosis.
Comments:
Reference: HP:0005897
Genes and Diseases:
 
       Child Nodes:

 Sister Nodes: 
..expandModerate generalized osteoporosis (HP:0005653) 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:0005897HP:0005897Severe generalized osteoporosis0COL1A1 CL E G H12772197OMIM:259420Osteogenesis imperfecta, type III.373
HP:0005897HP:0005897Severe generalized osteoporosis0COL1A2 CL E G H12782198OMIM:259420Osteogenesis imperfecta, type III.243


Genes (2) :COL1A1 COL1A2

Diseases (1) :OMIM:259420
 

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