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773750003: Flat face, microstomia, ear anomaly 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
3726270013 Simosa Penchaszadeh Bustos syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
3726271012 Blepharophimosis, telecanthus, microstomia syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3726272017 Flat face, microstomia, ear anomaly syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3726273010 Flat face, microstomia, ear anomaly syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
3726274016 Simosa craniofacial 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
Flat face, microstomia, ear anomaly syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Flat face, microstomia, ear anomaly syndrome Associated morphology Congenital smallness true Inferred relationship Existential restriction modifier 3
Flat face, microstomia, ear anomaly syndrome Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Flat face, microstomia, ear anomaly syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Flat face, microstomia, ear anomaly syndrome Finding site Face structure true Inferred relationship Existential restriction modifier 1
Flat face, microstomia, ear anomaly syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Flat face, microstomia, ear anomaly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Flat face, microstomia, ear anomaly syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Flat face, microstomia, ear anomaly syndrome Is a Microstomia true Inferred relationship Existential restriction modifier
Flat face, microstomia, ear anomaly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Flat face, microstomia, ear anomaly syndrome Finding site Mouth region structure true Inferred relationship Existential restriction modifier 3
Flat face, microstomia, ear anomaly syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Flat face, microstomia, ear anomaly syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 1
Flat face, microstomia, ear anomaly syndrome Is a Congenital malformation of ear true Inferred relationship Existential restriction modifier
Flat face, microstomia, ear anomaly syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Flat face, microstomia, ear anomaly syndrome Is a Auditory system hereditary disorder true Inferred relationship Existential restriction modifier
Flat face, microstomia, ear anomaly syndrome Finding site Ear structure true Inferred relationship Existential restriction modifier 2
Flat face, microstomia, ear anomaly syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Flat face, microstomia, ear anomaly 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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