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14870002: Achondrogenesis, type IB (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
25257011 Achondrogenesis, type IB en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
741311019 Achondrogenesis, type IB (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
931571000172115 achondrogenèse type 1B fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
1011361000172117 achondrogenèse type Parenti-Fraccaro fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
942881000172111 achondrogenesie type 1B nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
992281000172116 achondrogenesie, Parenti-Fraccaro-type nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Achondrogenesis, type IB Is a Achondrogenesis true Inferred relationship Some
Achondrogenesis, type IB Finding site Both upper extremities false Inferred relationship Some
Achondrogenesis, type IB Occurrence Congenital false Inferred relationship Some
Achondrogenesis, type IB Finding site Both lower extremities false Inferred relationship Some
Achondrogenesis, type IB Finding site Bone structure true Inferred relationship Some 1
Achondrogenesis, type IB Finding site Skeletal system structure false Inferred relationship Some 1
Achondrogenesis, type IB Associated morphology Congenital dysplasia false Inferred relationship Some 1
Achondrogenesis, type IB Associated morphology Congenital dysplasia false Inferred relationship Some 1
Achondrogenesis, type IB Finding site Bone structure false Inferred relationship Some 1
Achondrogenesis, type IB Occurrence Congenital true Inferred relationship Some 2
Achondrogenesis, type IB Associated morphology Dysplasia true Inferred relationship Some 2
Achondrogenesis, type IB Finding site Bone structure false Inferred relationship Some 2
Achondrogenesis, type IB Associated morphology Congenital dysplasia false Inferred relationship Some 2
Achondrogenesis, type IB Occurrence Congenital false Inferred relationship Some 3
Achondrogenesis, type IB Associated morphology Congenital hypoplasia false Inferred relationship Some 3
Achondrogenesis, type IB Finding site Bone structure false Inferred relationship Some 3
Achondrogenesis, type IB Occurrence Congenital true Inferred relationship Some 1
Achondrogenesis, type IB Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Achondrogenesis, type IB Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Achondrogenesis, type IB Associated morphology Hypoplasia true Inferred relationship Some 1
Achondrogenesis, type IB Finding site Skeletal system structure true Inferred relationship Some 2
Achondrogenesis, type IB Is a Congenital anomaly of skeletal bone true Inferred relationship Some
Achondrogenesis, type IB Interprets Height / growth measure true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

GB English

US English

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