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1220597000: Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome (disorder)


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

Descriptions:

Id Description Lang Type Status Case? Module
5045345015 Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5045346019 Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
5045347011 Retinal dystrophy, juvenile cataract, short stature syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
5045348018 A rare genetic syndromic rod-cone dystrophy disorder with characteristics of psychomotor developmental delay from early childhood, intellectual disability, short stature, mild facial dysmorphism (e.g. upslanted palpebral fissures, hypoplastic alae nasi, malar hypoplasia, attached earlobes), excessive dental spacing and malocclusion, juvenile cataract and ophthalmologic findings of atypical retinitis pigmentosa (i.e. salt-and-pepper retinopathy, attenuated retinal arterioles, generalised rod-cone dysfunction, mottled macula, peripapillary sparing of retinal pigment epithelium). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5045349014 A rare genetic syndromic rod-cone dystrophy disorder with characteristics of psychomotor developmental delay from early childhood, intellectual disability, short stature, mild facial dysmorphism (e.g. upslanted palpebral fissures, hypoplastic alae nasi, malar hypoplasia, attached earlobes), excessive dental spacing and malocclusion, juvenile cataract and ophthalmologic findings of atypical retinitis pigmentosa (i.e. salt-and-pepper retinopathy, attenuated retinal arterioles, generalized rod-cone dysfunction, mottled macula, peripapillary sparing of retinal pigment epithelium). 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
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Is a Intellectual disability true Inferred relationship Some
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Is a Autosomal recessive retinitis pigmentosa true Inferred relationship Some
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Is a Short stature disorder true Inferred relationship Some
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Is a Juvenile cataract (disorder) true Inferred relationship Some
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Interprets Body height (observable entity) true Inferred relationship Some 4
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Has interpretation Below reference range true Inferred relationship Some 4
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Occurrence Congenital true Inferred relationship Some 3
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Finding site Face structure true Inferred relationship Some 3
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Finding site Lens clear true Inferred relationship Some 1
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Associated morphology Opacity true Inferred relationship Some 1
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Finding site Retinal structure true Inferred relationship Some 2
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Associated morphology Dystrophy true Inferred relationship Some 2
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Interprets Adaptation behavior (observable entity) true Inferred relationship Some 5
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Has interpretation Impaired true Inferred relationship Some 5
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Interprets Intellectual ability (observable entity) true Inferred relationship Some 6
Retinitis pigmentosa, juvenile cataract, short stature, intellectual disability syndrome Has interpretation Impaired true Inferred relationship Some 6

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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