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718575002: Ablepharon macrostomia syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3312810019 Ablepharon macrostomia syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3312816013 Ablepharon macrostomia syndrome en Synonym Active Case insensitive SNOMED CT core
3312817016 An extremely rare multiple congenital malformation syndrome with the association of ablepharon, macrostomia, abnormal external ears, syndactyly of the hands and feet, skin findings (such as dry and coarse skin or redundant folds of skin), absent or sparse hair, genital malformations and developmental delay in two thirds of cases. Other reported manifestations include malar hypoplasia, absent or hypoplastic nipples, umbilical abnormalities and growth retardation. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ablepharon macrostomia syndrome Associated morphology Congenital absence false Inferred relationship Some 1
Ablepharon macrostomia syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
Ablepharon macrostomia syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Ablepharon macrostomia syndrome Occurrence Congenital true Inferred relationship Some 1
Ablepharon macrostomia syndrome Finding site Eyelid structure true Inferred relationship Some 1
Ablepharon macrostomia syndrome Is a Hereditary disorder of musculoskeletal system false Inferred relationship Some
Ablepharon macrostomia syndrome Pathological process Pathological developmental process false Inferred relationship Some 4
Ablepharon macrostomia syndrome Finding site Bone structure of head false Inferred relationship Some 4
Ablepharon macrostomia syndrome Associated morphology Developmental failure of fusion false Inferred relationship Some 4
Ablepharon macrostomia syndrome Is a Developmental hereditary disorder true Inferred relationship Some
Ablepharon macrostomia syndrome Associated morphology Absence true Inferred relationship Some 1
Ablepharon macrostomia syndrome Due to Congenital failure of fusion between maxillary and mandibular processes true Inferred relationship Some 3
Ablepharon macrostomia syndrome Is a Autosomal dominant hereditary disorder true Inferred relationship Some
Ablepharon macrostomia syndrome Is a Ablepharon true Inferred relationship Some
Ablepharon macrostomia syndrome Is a Congenital macrostomia true Inferred relationship Some
Ablepharon macrostomia syndrome Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Some
Ablepharon macrostomia syndrome Is a Digestive system hereditary disorder true Inferred relationship Some
Ablepharon macrostomia syndrome Is a Hereditary disorder of the visual system true Inferred relationship Some
Ablepharon macrostomia syndrome Associated morphology Developmental failure of fusion false Inferred relationship Some 3
Ablepharon macrostomia syndrome Occurrence Congenital false Inferred relationship Some 3
Ablepharon macrostomia syndrome Finding site Structure of internal part of mouth false Inferred relationship Some 3
Ablepharon macrostomia syndrome Associated morphology Congenital absence false Inferred relationship Some 4
Ablepharon macrostomia syndrome Occurrence Congenital false Inferred relationship Some 4
Ablepharon macrostomia syndrome Finding site Eyelid structure false Inferred relationship Some 4
Ablepharon macrostomia syndrome Associated morphology Developmental failure of fusion true Inferred relationship Some 2
Ablepharon macrostomia syndrome Occurrence Congenital true Inferred relationship Some 2
Ablepharon macrostomia syndrome Finding site Structure of oral region of face true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Queensland allied health clinical finding reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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