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773667003: Hypertelorism, preauricular sinus, punctual pits, deafness syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jan 2019. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3725585011 Hypertelorism, preauricular sinus, punctual pits, deafness syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3725586012 Hypertelorism, preauricular sinus, punctual pits, deafness syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3725587015 HPPD (hypertelorism, preauricular sinus, punctual pits, deafness) syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3725588013 Hypertelorism, preauricular sinus, punctual pits, hearing loss 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
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Finding site Preauricular region structure true Inferred relationship Existential restriction modifier 1
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Is a Hypertelorism true Inferred relationship Existential restriction modifier
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Is a Hearing loss associated with syndrome true Inferred relationship Existential restriction modifier
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Associated morphology Preauricular sinus true Inferred relationship Existential restriction modifier 1
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Is a Preauricular fistula true Inferred relationship Existential restriction modifier
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Finding site Ear structure true Inferred relationship Existential restriction modifier 3
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Finding site Sphenoid bone structure true Inferred relationship Existential restriction modifier 2
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Is a Multiple system malformation syndrome true Inferred relationship Existential restriction modifier
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Is a Disorder of ear true Inferred relationship Existential restriction modifier
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 4
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Is a Congenital hearing disorder true Inferred relationship Existential restriction modifier
Hypertelorism, preauricular sinus, punctual pits, deafness syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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