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718575002: Ablepharon macrostomia 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
3312810019 Ablepharon macrostomia syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
3312816013 Ablepharon macrostomia 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
Ablepharon macrostomia syndrome Due to Congenital failure of fusion between maxillary and mandibular processes true Inferred relationship Existential restriction modifier 3
Ablepharon macrostomia syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Existential restriction modifier
Ablepharon macrostomia syndrome Is a Ablepharon true Inferred relationship Existential restriction modifier
Ablepharon macrostomia syndrome Is a Congenital macrostomia true Inferred relationship Existential restriction modifier
Ablepharon macrostomia syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier
Ablepharon macrostomia syndrome Is a Digestive system hereditary disorder true Inferred relationship Existential restriction modifier
Ablepharon macrostomia syndrome Is a Hereditary disorder of the visual system true Inferred relationship Existential restriction modifier
Ablepharon macrostomia syndrome Associated morphology Developmental failure of fusion false Inferred relationship Existential restriction modifier 3
Ablepharon macrostomia syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 3
Ablepharon macrostomia syndrome Finding site Structure of region of internal part of mouth false Inferred relationship Existential restriction modifier 3
Ablepharon macrostomia syndrome Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 4
Ablepharon macrostomia syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier 4
Ablepharon macrostomia syndrome Finding site Eyelid structure false Inferred relationship Existential restriction modifier 4
Ablepharon macrostomia syndrome Associated morphology Developmental failure of fusion true Inferred relationship Existential restriction modifier 2
Ablepharon macrostomia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Ablepharon macrostomia syndrome Finding site Structure of oral region of face true Inferred relationship Existential restriction modifier 2
Ablepharon macrostomia syndrome Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Ablepharon macrostomia syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Ablepharon macrostomia syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Ablepharon macrostomia syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Ablepharon macrostomia syndrome Finding site Eyelid structure true Inferred relationship Existential restriction modifier 1
Ablepharon macrostomia syndrome Is a Hereditary disorder of musculoskeletal system false Inferred relationship Existential restriction modifier
Ablepharon macrostomia syndrome Pathological process Pathological developmental process false Inferred relationship Existential restriction modifier 4
Ablepharon macrostomia syndrome Finding site Bone structure of head false Inferred relationship Existential restriction modifier 4
Ablepharon macrostomia syndrome Associated morphology Developmental failure of fusion false Inferred relationship Existential restriction modifier 4
Ablepharon macrostomia syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Ablepharon macrostomia syndrome Associated morphology Absence true Inferred relationship Existential restriction modifier 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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