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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. Date: 31-Jul 2003. Module: SNOMED CT core module

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 SNOMED CT core module
1782578011 Aplasia cutis congenita secondary to malformation syndrome (Type 9) en Synonym Active Only initial character case insensitive SNOMED CT core 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) Is a Aplasia cutis congenita true Inferred relationship Existential restriction modifier
Aplasia cutis congenita secondary to malformation syndrome (Type 9) Finding site Structure of skin region false Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) Occurrence Congenital false Inferred relationship Existential restriction modifier
Aplasia cutis congenita secondary to malformation syndrome (Type 9) Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) Associated with Congenital malformation syndrome true Inferred relationship Existential restriction modifier 2
Aplasia cutis congenita secondary to malformation syndrome (Type 9) Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) Occurrence Congenital false Inferred relationship Existential restriction modifier 2
Aplasia cutis congenita secondary to malformation syndrome (Type 9) Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Aplasia cutis congenita secondary to malformation syndrome (Type 9) Associated morphology Congenital partial absence false Inferred relationship Existential restriction modifier 2
Aplasia cutis congenita secondary to malformation syndrome (Type 9) Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) Associated morphology Congenital absence false Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) Finding site Skin part true Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Aplasia cutis congenita secondary to malformation syndrome (Type 9) Associated morphology Aplasia true Inferred relationship Existential restriction modifier 1
Inbound Relationships Type Active Source Characteristic Refinability Group
Oculocerebrocutaneous syndrome Is a True Aplasia cutis congenita secondary to malformation syndrome (Type 9) Inferred relationship Existential restriction modifier

This concept is not in any reference sets

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