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201131000146109: syndroom van congenitale spierdystrofie, infantiel cataract en hypogonadisme bij man (aandoening)


Status: current, Sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2022. Module: SNOMED CT Netherlands NRC maintained module (core metadata concept)

Descriptions:

Id Description Lang Type Status Case? Module
13509821000146118 Male congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13509841000146112 Male congenital muscular dystrophy with infantile cataract and hypogonadism syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13509811000146111 syndroom van congenitale spierdystrofie, infantiel cataract en hypogonadisme bij man nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13509831000146116 congenitale spierdystrofie met infantiel cataract en hypogonadisme bij man nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13509851000146110 syndroom van congenitale spierdystrofie, infantiel cataract en hypogonadisme bij man (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Male congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) Is a Male hypogonadism true Inferred relationship Some
Male congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) Is a Congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) true Inferred relationship Some
Male congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) Is a Disorder of endocrine testis false Inferred relationship Some
Male congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) Clinical course Progressive (qualifier value) true Inferred relationship Some 3
Male congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Male congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) Finding site Skeletal muscle structure true Inferred relationship Some 1
Male congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) Associated morphology Dystrophy true Inferred relationship Some 1
Male congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Male congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
Male congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) Finding site Testicular endocrine structure true Inferred relationship Some 2
Male congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) Occurrence Infancy true Inferred relationship Some 4
Male congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) Finding site Lens clear true Inferred relationship Some 4
Male congenital muscular dystrophy with infantile cataract and hypogonadism syndrome (disorder) Associated morphology Opacity true Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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