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722108000: Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2017. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3330721019 Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3330722014 Osteochondrodysplatic nanism, deafness, retinitis pigmentosa 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
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Is a Sensorineural hearing loss true Inferred relationship Existential restriction modifier
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Is a Congenital hearing disorder false Inferred relationship Existential restriction modifier
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Is a Autosomal dominant retinitis pigmentosa true Inferred relationship Existential restriction modifier
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Is a Short stature disorder true Inferred relationship Existential restriction modifier
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Is a Osteochondrodysplasia false Inferred relationship Existential restriction modifier
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Finding site Structure of auditory system true Inferred relationship Existential restriction modifier 3
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 4
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Interprets Functional observable false Inferred relationship Existential restriction modifier
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Associated morphology Dystrophy false Inferred relationship Existential restriction modifier 7
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 7
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Finding site Retinal structure false Inferred relationship Existential restriction modifier 7
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 8
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 8
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Finding site Bone structure false Inferred relationship Existential restriction modifier 8
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Is a Congenital anomaly of retina true Inferred relationship Existential restriction modifier
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Associated morphology Congenital dysplasia false Inferred relationship Existential restriction modifier 1
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Finding site Retinal structure true Inferred relationship Existential restriction modifier 2
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Associated morphology Dystrophy true Inferred relationship Existential restriction modifier 2
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Finding site Bone structure true Inferred relationship Existential restriction modifier 1
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Is a Congenital skeletal dysplasia true Inferred relationship Existential restriction modifier
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Is a Congenital anomaly of skeletal bone true Inferred relationship Existential restriction modifier
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Osteochondrodysplatic nanism, deafness, retinitis pigmentosa syndrome Interprets Height / growth measure true Inferred relationship Existential restriction modifier 5

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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