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1172605003: Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 30-Sep 2021. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
4634562016 Retinitis pigmentosa, deafness, premature aging, short stature, facial dysmorphism syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
4634563014 Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
4634564015 Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
4634565019 Retinitis pigmentosa, hearing loss, premature ageing, short stature, facial dysmorphism syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
4634566018 Retinitis pigmentosa, deafness, premature ageing, short stature, facial dysmorphism syndrome en Synonym Active Entire term case insensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Is a Autosomal recessive retinitis pigmentosa true Inferred relationship Existential restriction modifier
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Existential restriction modifier
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Is a Disorder of stature true Inferred relationship Existential restriction modifier
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Is a Premature aging syndrome true Inferred relationship Existential restriction modifier
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Is a Brachydactyly true Inferred relationship Existential restriction modifier
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Is a Sensorineural hearing loss true Inferred relationship Existential restriction modifier
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Finding site Structure of auditory system true Inferred relationship Existential restriction modifier 4
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Finding site Skin structure true Inferred relationship Existential restriction modifier 6
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 3
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 3
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Finding site Digit structure true Inferred relationship Existential restriction modifier 1
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Associated morphology Abnormally short growth true Inferred relationship Existential restriction modifier 1
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 5
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 5
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 5
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 5
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Finding site Retinal structure true Inferred relationship Existential restriction modifier 2
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 2
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Interprets Body height measure true Inferred relationship Existential restriction modifier 7
Retinitis pigmentosa, hearing loss, premature aging, short stature, facial dysmorphism syndrome Has interpretation Below reference range true Inferred relationship Existential restriction modifier 7

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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