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205468002: Hypochondroplasia (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
315057016 Hypochondroplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
315058014 Hypochondrodysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
590839019 Hypochondroplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
315057016 Hypochondroplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
315057016 Hypochondroplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
315058014 Hypochondrodysplasia en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
315058014 Hypochondrodysplasia en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
590839019 Hypochondroplasia (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
590839019 Hypochondroplasia (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3455391001000119 Hypochondroplasie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
969481000172112 hypochondroplasie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
969481000172112 hypochondroplasie fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3455391001000119 Hypochondroplasie de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Hypochondroplasia Is a Skeletal dysplasia true Inferred relationship Existential restriction modifier (core metadata concept)
Hypochondroplasia Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypochondroplasia Finding site Bone structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypochondroplasia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Hypochondroplasia Finding site Skeletal system structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypochondroplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypochondroplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypochondroplasia Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypochondroplasia Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypochondroplasia Finding site Bone structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypochondroplasia Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier (core metadata concept) 2
Hypochondroplasia Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypochondroplasia Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Hypochondroplasia Is a Congenital malformation syndromes associated with short stature true Inferred relationship Existential restriction modifier (core metadata concept)
Hypochondroplasia Is a Congenital anomaly of skeletal bone true Inferred relationship Existential restriction modifier (core metadata concept)
Hypochondroplasia Interprets Height / growth measure (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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