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1208746001: syndroom van verstandelijke beperking, spierzwakte, kleine gestalte en faciale dysmorfie (aandoening)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Mar 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
4970752014 Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4970753016 Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
13587401000146119 syndroom van mentale retardatie, spierzwakte, dwerggroei en faciale dysmorfie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13587411000146117 syndroom van verstandelijke beperking, spierzwakte, kleine gestalte en faciale dysmorfie (aandoening) nl Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13587421000146110 syndroom van verstandelijke handicap, spierzwakte, kleine gestalte en dysmorfie van aangezicht nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
13587431000146112 syndroom van verstandelijke beperking, spierzwakte, kleine gestalte en faciale dysmorfie nl Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Netherlands NRC maintained module (core metadata concept)
4970754010 A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of intellectual disability, developmental delay, delayed bone age, short stature, generalized muscle weakness and dysmorphic facial features (such as high arched eyebrows, downslanting palpebral fissures, prominent nose and narrow palate and mouth). Additional reported manifestations include blue sclerae, ophthalmoplegia and intention tremor. Brain imaging may show white matter abnormalities. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
4970755011 A rare genetic multiple congenital anomalies/dysmorphic syndrome with characteristics of intellectual disability, developmental delay, delayed bone age, short stature, generalised muscle weakness and dysmorphic facial features (such as high arched eyebrows, downslanting palpebral fissures, prominent nose and narrow palate and mouth). Additional reported manifestations include blue sclerae, ophthalmoplegia and intention tremor. Brain imaging may show white matter abnormalities. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Is a Intellectual disability true Inferred relationship Some
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Is a Delayed bone age true Inferred relationship Some
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Is a Short stature disorder true Inferred relationship Some
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Is a Developmental delay true Inferred relationship Some
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Is a Muscle weakness true Inferred relationship Some
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Is a Disorder of skeletal muscle true Inferred relationship Some
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Is a Disorder of bone (disorder) true Inferred relationship Some
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Is a Genetic disease true Inferred relationship Some
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Finding site Skeletal muscle structure true Inferred relationship Some 2
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Finding site Bone structure true Inferred relationship Some 3
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Occurrence Congenital true Inferred relationship Some 1
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Finding site Face structure true Inferred relationship Some 1
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Interprets Body height measure (observable entity) true Inferred relationship Some 4
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Has interpretation Below reference range true Inferred relationship Some 4
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Interprets Adaptation behavior (observable entity) true Inferred relationship Some 5
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Has interpretation Impaired true Inferred relationship Some 5
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Interprets Intellectual ability (observable entity) true Inferred relationship Some 6
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Has interpretation Impaired true Inferred relationship Some 6
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Is a Movement disorder true Inferred relationship Some
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Interprets Movement false Inferred relationship Some 5
Intellectual disability, muscle weakness, short stature, facial dysmorphism syndrome Interprets Movement true Inferred relationship Some 7

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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