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403553002: Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1771479014 Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1782578011 Aplasia cutis congenita secondary to malformation syndrome (Type 9) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1771479014 Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1782578011 Aplasia cutis congenita secondary to malformation syndrome (Type 9) en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5815331000241119 aplasie cutanée congénitale de type 9 secondaire à un syndrome malformatif fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5815341000241112 ACC (aplasia cutis congenita) de type 9 secondaire à un syndrome malformatif fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5815351000241110 aplasie congénitale de la peau de type 9 secondaire à un syndrome malformatif fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5815331000241119 aplasie cutanée congénitale de type 9 secondaire à un syndrome malformatif fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5815341000241112 ACC (aplasia cutis congenita) de type 9 secondaire à un syndrome malformatif fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5815351000241110 aplasie congénitale de la peau de type 9 secondaire à un syndrome malformatif fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module

1 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) Is a Aplasia cutis congenita (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) Finding site Structure of skin region (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) Associated with Congenital malformation syndrome true Inferred relationship Existential restriction modifier (core metadata concept) 2
Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 2
Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) Associated morphology Congenital partial absence false Inferred relationship Existential restriction modifier (core metadata concept) 2
Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Existential restriction modifier (core metadata concept) 1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) Finding site Skin part (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) Associated morphology Aplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Oculocerebrocutaneous syndrome (disorder) Is a True Aplasia cutis congenita secondary to malformation syndrome (Type 9) (disorder) Inferred relationship Existential restriction modifier (core metadata concept)

This concept is not in any reference sets

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