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720499004: Aplasia cutis with myopia syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3321035010 Aplasia cutis with myopia syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3321036011 Aplasia cutis with myopia syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3321037019 Gershoni Baruch Leibo syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3321038012 This syndrome has characteristics of the association of aplasia cutis congenita with high myopia, congenital nystagmus and cone-rod dysfunction. It has been described in two siblings (brother and sister). Transmission is autosomal dominant. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Aplasia cutis with myopia syndrome (disorder) Is a Severe myopia true Inferred relationship Some
Aplasia cutis with myopia syndrome (disorder) Is a Aplasia cutis congenita true Inferred relationship Some
Aplasia cutis with myopia syndrome (disorder) Is a Multiple system malformation syndrome true Inferred relationship Some
Aplasia cutis with myopia syndrome (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Aplasia cutis with myopia syndrome (disorder) Is a Hereditary disorder of the integument true Inferred relationship Some
Aplasia cutis with myopia syndrome (disorder) Is a Hereditary disorder of the visual system (disorder) true Inferred relationship Some
Aplasia cutis with myopia syndrome (disorder) Finding site Structure of visual system (body structure) false Inferred relationship Some
Aplasia cutis with myopia syndrome (disorder) Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Some 2
Aplasia cutis with myopia syndrome (disorder) Occurrence Congenital false Inferred relationship Some 2
Aplasia cutis with myopia syndrome (disorder) Finding site Skin part false Inferred relationship Some 2
Aplasia cutis with myopia syndrome (disorder) Finding site Structure of visual system (body structure) true Inferred relationship Some 2
Aplasia cutis with myopia syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Aplasia cutis with myopia syndrome (disorder) Finding site Skin part true Inferred relationship Some 1
Aplasia cutis with myopia syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Aplasia cutis with myopia syndrome (disorder) Occurrence Congenital true Inferred relationship Some 1
Aplasia cutis with myopia syndrome (disorder) Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Some 1
Aplasia cutis with myopia syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Some
Aplasia cutis with myopia syndrome (disorder) Associated morphology Aplasia true Inferred relationship Some 1

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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