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763774001: Keipert syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2018. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module
3643795014 Keipert syndrome (disorder) en Fully specified name Active Entire term case sensitive SNOMED CT core module
3643796010 Nasodigitoacoustic syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3643797018 Keipert 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
Keipert syndrome Is a Congenital anomaly of skeletal bone true Inferred relationship Existential restriction modifier
Keipert syndrome Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Existential restriction modifier
Keipert syndrome Is a Hearing loss associated with syndrome true Inferred relationship Existential restriction modifier
Keipert syndrome Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Keipert syndrome Is a Connective tissue hereditary disorder false Inferred relationship Existential restriction modifier
Keipert syndrome Is a Hereditary disorder of musculoskeletal system true Inferred relationship Existential restriction modifier
Keipert syndrome Is a Congenital sensorineural hearing loss true Inferred relationship Existential restriction modifier
Keipert syndrome Interprets Hearing, function true Inferred relationship Existential restriction modifier 4
Keipert syndrome Interprets Functional observable false Inferred relationship Existential restriction modifier
Keipert syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Keipert syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Keipert syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Keipert syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Keipert syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 2
Keipert syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Keipert syndrome Finding site Bone structure of extremity true Inferred relationship Existential restriction modifier 1
Keipert syndrome Finding site Ear structure true Inferred relationship Existential restriction modifier 3
Keipert syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Keipert syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Keipert syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Keipert syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Keipert syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Keipert syndrome Is a Disorder of ear true Inferred relationship Existential restriction modifier
Keipert 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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