Human Disease Ontology

Last uploaded: June 2, 2024
Preferred Name

osteogenesis imperfecta type 3

Synonyms

OI3

Definitions

An osteogenesis imperfecta that is characterized by progressive limb and spinal deformity and normal sclerae and has_material_basis_in mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3.

ID

http://purl.obolibrary.org/obo/DOID_0110339

database_cross_reference

ICD10CM:Q78.0

GARD:8695

MIM:259420

definition

An osteogenesis imperfecta that is characterized by progressive limb and spinal deformity and normal sclerae and has_material_basis_in mutations in the COL1A1 gene on chromosome 17q21.33 or the COL1A2 gene on chromosome 7q21.3.

has exact synonym

OI3

osteogenesis imperfecta type III

progressively deforming osteogenesis imperfecta with normal sclera

has material basis in

http://purl.obolibrary.org/obo/GENO_0000147

has_obo_namespace

disease_ontology

id

DOID:0110339

in_subset

http://purl.obolibrary.org/obo/doid#DO_rare_slim

label

osteogenesis imperfecta type 3

notation

DOID:0110339

prefLabel

osteogenesis imperfecta type 3

subClassOf

http://purl.obolibrary.org/obo/DOID_12347

http://purl.obolibrary.org/obo/DOID_0050736

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