75654009: Benign autosomal dominant osteopetrosis (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 28-Feb 2023. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

125655011 Benign autosomal dominant osteopetrosis en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

816288011 Benign autosomal dominant osteopetrosis (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

5510921000172119 ostéopétrose autosomique dominante bénigne fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

5510931000172116 benigne autosomaal dominante osteopetrose nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) Belgian module (core metadata concept)

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
ostéopétrose autosomique dominante bénigne	Is a	Osteopetrosis	false	Inferred relationship	Some
ostéopétrose autosomique dominante bénigne	Is a	Hereditary disorder of musculoskeletal system	false	Inferred relationship	Some
ostéopétrose autosomique dominante bénigne	Is a	Autosomal dominant hereditary disorder	false	Inferred relationship	Some
ostéopétrose autosomique dominante bénigne	Occurrence	Congenital	false	Inferred relationship	Some
ostéopétrose autosomique dominante bénigne	Finding site	Bone structure	false	Inferred relationship	Some	1
ostéopétrose autosomique dominante bénigne	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	1
ostéopétrose autosomique dominante bénigne	Is a	Connective tissue hereditary disorder (disorder)	false	Inferred relationship	Some
ostéopétrose autosomique dominante bénigne	Finding site	Bone structure	false	Inferred relationship	Some	1
ostéopétrose autosomique dominante bénigne	Associated morphology	Congenital anomaly	false	Inferred relationship	Some	1
ostéopétrose autosomique dominante bénigne	Occurrence	Congenital	false	Inferred relationship	Some	2
ostéopétrose autosomique dominante bénigne	Associated morphology	Developmental anomaly	false	Inferred relationship	Some	2
ostéopétrose autosomique dominante bénigne	Finding site	Bone structure	false	Inferred relationship	Some	2
ostéopétrose autosomique dominante bénigne	Occurrence	Congenital	false	Inferred relationship	Some	1
ostéopétrose autosomique dominante bénigne	Associated morphology	Morphologically abnormal structure (morphologic abnormality)	false	Inferred relationship	Some	1
ostéopétrose autosomique dominante bénigne	Pathological process (attribute)	Pathological developmental process	false	Inferred relationship	Some	1
ostéopétrose autosomique dominante bénigne	Has interpretation	Below reference range	false	Inferred relationship	Some	2
ostéopétrose autosomique dominante bénigne	Interprets	Osteoclast turnover rate	false	Inferred relationship	Some	2
ostéopétrose autosomique dominante bénigne	Clinical course	Progressive (qualifier value)	false	Inferred relationship	Some	3

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)