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721087008: Deafness and intellectual disability Martin Probst type 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
3323439015 Deafness and intellectual disability Martin Probst type syndrome (disorder) en Fully specified name Active Only initial character case insensitive SNOMED CT core module
3323440018 Deafness and intellectual disability Martin Probst type syndrome en Synonym Active Only initial character case insensitive SNOMED CT core module
3323441019 Martin Probst syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3323442014 X-linked deafness and intellectual disability syndrome en Synonym Active Entire term case sensitive SNOMED CT core module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Deafness and intellectual disability Martin Probst type syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Deafness and intellectual disability Martin Probst type syndrome Is a Mental retardation false Inferred relationship Existential restriction modifier
Deafness and intellectual disability Martin Probst type syndrome Is a Bilateral hearing loss true Inferred relationship Existential restriction modifier
Deafness and intellectual disability Martin Probst type syndrome Is a Congenital hearing disorder false Inferred relationship Existential restriction modifier
Deafness and intellectual disability Martin Probst type syndrome Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
Deafness and intellectual disability Martin Probst type syndrome Is a Hearing loss associated with syndrome true Inferred relationship Existential restriction modifier
Deafness and intellectual disability Martin Probst type syndrome Is a Auditory system hereditary disorder false Inferred relationship Existential restriction modifier
Deafness and intellectual disability Martin Probst type syndrome Finding site Ear structure false Inferred relationship Existential restriction modifier 2
Deafness and intellectual disability Martin Probst type syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 3
Deafness and intellectual disability Martin Probst type syndrome Interprets Functional observable false Inferred relationship Existential restriction modifier
Deafness and intellectual disability Martin Probst type syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 4
Deafness and intellectual disability Martin Probst type syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Deafness and intellectual disability Martin Probst type syndrome Finding site Face structure false Inferred relationship Existential restriction modifier 4
Deafness and intellectual disability Martin Probst type syndrome Is a Intellectual disability true Inferred relationship Existential restriction modifier
Deafness and intellectual disability Martin Probst type syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Deafness and intellectual disability Martin Probst type syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Deafness and intellectual disability Martin Probst type syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 1
Deafness and intellectual disability Martin Probst type syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Deafness and intellectual disability Martin Probst type syndrome Finding site Structure of auditory system true Inferred relationship Existential restriction modifier 2
Deafness and intellectual disability Martin Probst type syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Deafness and intellectual disability Martin Probst type syndrome Is a X-linked recessive hereditary disease true Inferred relationship Existential restriction modifier
Deafness and intellectual disability Martin Probst type syndrome Is a Congenital sensorineural hearing loss true Inferred relationship Existential restriction modifier
Deafness and intellectual disability Martin Probst type syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 3
Deafness and intellectual disability Martin Probst type syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Deafness and intellectual disability Martin Probst type syndrome Is a X-linked sensorineural hearing loss true Inferred relationship Existential restriction modifier
Deafness and intellectual disability Martin Probst type syndrome Interprets Intellectual ability true Inferred relationship Existential restriction modifier 4
Deafness and intellectual disability Martin Probst type syndrome Has interpretation Impaired true Inferred relationship Existential restriction modifier 4
Deafness and intellectual disability Martin Probst type syndrome Interprets Adaptation behavior true Inferred relationship Existential restriction modifier 5
Deafness and intellectual disability Martin Probst type syndrome Has interpretation Impaired 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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