22932004: Chondrodysplasia punctata, Conradi-Hünermann type (disorder)

Status: retired, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

38517016 Chondrodysplasia punctata, Conradi-Hünermann type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

38518014 Conradi-Hünermann syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

38519018 Conradi's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

38520012 Chondrodysplasia punctata, Conradi-Hunermann type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

38521011 Conradi-Hunermann syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core

481474011 Chondrodysplasia punctata, X-linked dominant type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core

481475012 Chondrodysplasia calcificans congenita en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core

752396018 Chondrodysplasia punctata, Conradi-Hünermann type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Chondrodysplasia punctata, Conradi-Hünermann type	Is a	Chondrodysplasia punctata	false	Inferred relationship	Some
Chondrodysplasia punctata, Conradi-Hünermann type	Is a	Cutaneous syndrome with ichthyosis	false	Inferred relationship	Some
Chondrodysplasia punctata, Conradi-Hünermann type	Is a	Hereditary disorder of musculoskeletal system	false	Inferred relationship	Some
Chondrodysplasia punctata, Conradi-Hünermann type	Occurrence	Congenital	false	Inferred relationship	Some
Chondrodysplasia punctata, Conradi-Hünermann type	Finding site	Bone structure	false	Inferred relationship	Some	2
Chondrodysplasia punctata, Conradi-Hünermann type	Finding site	Structure of skin region	false	Inferred relationship	Some
Chondrodysplasia punctata, Conradi-Hünermann type	Associated morphology	Dysplasia	false	Inferred relationship	Some	1
Chondrodysplasia punctata, Conradi-Hünermann type	Finding site	Skeletal system structure	false	Inferred relationship	Some	1
Chondrodysplasia punctata, Conradi-Hünermann type	Associated morphology	Congenital dysplasia	false	Inferred relationship	Some	2

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

Reference Sets

Concept inactivation indicator reference set

POSSIBLY EQUIVALENT TO association reference set (foundation metadata concept)