403554008: Oculocerebrocutaneous syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\...

\Aplasia of skin\Aplasia cutis congenita\Aplasia cutis congenita secondary to malformation syndrome (Type 9)\Oculocerebrocutaneous syndrome

\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis congenita secondary to malformation syndrome (Type 9)\Oculocerebrocutaneous syndrome

\General finding of soft tissue\Skin finding\Disorder of skin\Aplasia of skin\Aplasia cutis congenita\Aplasia cutis congenita secondary to malformation syndrome (Type 9)\Oculocerebrocutaneous syndrome
\General finding of soft tissue\Skin finding\Disorder of skin\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis congenita secondary to malformation syndrome (Type 9)\Oculocerebrocutaneous syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Aplasia of skin\Aplasia cutis congenita\Aplasia cutis congenita secondary to malformation syndrome (Type 9)\Oculocerebrocutaneous syndrome
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis congenita secondary to malformation syndrome (Type 9)\Oculocerebrocutaneous syndrome

\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Aplasia of skin\Aplasia cutis congenita\Aplasia cutis congenita secondary to malformation syndrome (Type 9)\Oculocerebrocutaneous syndrome
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis congenita secondary to malformation syndrome (Type 9)\Oculocerebrocutaneous syndrome
\Integumentary system finding\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis congenita secondary to malformation syndrome (Type 9)\Oculocerebrocutaneous syndrome
\Integumentary system finding\Skin finding\Disorder of skin\Aplasia of skin\Aplasia cutis congenita\Aplasia cutis congenita secondary to malformation syndrome (Type 9)\Oculocerebrocutaneous syndrome
\Integumentary system finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis congenita secondary to malformation syndrome (Type 9)\Oculocerebrocutaneous syndrome

\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Aplasia of skin\Aplasia cutis congenita\Aplasia cutis congenita secondary to malformation syndrome (Type 9)\Oculocerebrocutaneous syndrome
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis congenita secondary to malformation syndrome (Type 9)\Oculocerebrocutaneous syndrome
\Disease\Disorder of body system\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis congenita secondary to malformation syndrome (Type 9)\Oculocerebrocutaneous syndrome
\Disease\Congenital disease\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis congenita secondary to malformation syndrome (Type 9)\Oculocerebrocutaneous syndrome
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Aplasia of skin\Aplasia cutis congenita\Aplasia cutis congenita secondary to malformation syndrome (Type 9)\Oculocerebrocutaneous syndrome
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis congenita secondary to malformation syndrome (Type 9)\Oculocerebrocutaneous syndrome
\Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Aplasia cutis congenita\Aplasia cutis congenita secondary to malformation syndrome (Type 9)\Oculocerebrocutaneous syndrome

Status: current, Primitive. Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module

2647588016 Delleman-Oorthuys syndrome en Synonym Active Case sensitive SNOMED CT core

4579830015 Oculocerebrocutaneous syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core

4579831016 Oculocerebrocutaneous syndrome en Synonym Active Case insensitive SNOMED CT core

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Oculocerebrocutaneous syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Some	1
Oculocerebrocutaneous syndrome	Associated morphology	Aplasia	true	Inferred relationship	Some	1
Oculocerebrocutaneous syndrome	Is a	Aplasia cutis congenita secondary to malformation syndrome (Type 9)	true	Inferred relationship	Some
Oculocerebrocutaneous syndrome	Occurrence	Congenital	false	Inferred relationship	Some
Oculocerebrocutaneous syndrome	Associated morphology	Congenital absence	false	Inferred relationship	Some	1
Oculocerebrocutaneous syndrome	Finding site	Structure of skin region	false	Inferred relationship	Some	1
Oculocerebrocutaneous syndrome	Associated with	Congenital malformation syndrome	true	Inferred relationship	Some	2
Oculocerebrocutaneous syndrome	Finding site	Skin structure	false	Inferred relationship	Some	1
Oculocerebrocutaneous syndrome	Associated morphology	Congenital absence	false	Inferred relationship	Some	1
Oculocerebrocutaneous syndrome	Finding site	Skin structure	false	Inferred relationship	Some	1
Oculocerebrocutaneous syndrome	Occurrence	Congenital	false	Inferred relationship	Some	2
Oculocerebrocutaneous syndrome	Finding site	Skin structure	false	Inferred relationship	Some	2
Oculocerebrocutaneous syndrome	Associated morphology	Congenital partial absence	false	Inferred relationship	Some	2
Oculocerebrocutaneous syndrome	Occurrence	Congenital	true	Inferred relationship	Some	1
Oculocerebrocutaneous syndrome	Associated morphology	Congenital absence	false	Inferred relationship	Some	1
Oculocerebrocutaneous syndrome	Finding site	Skin part	true	Inferred relationship	Some	1

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Microphthalmos due to Delleman syndrome	Due to	True	Oculocerebrocutaneous syndrome	Inferred relationship	Some	2

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

Description inactivation indicator reference set

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
2647588016	Delleman-Oorthuys syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
4579830015	Oculocerebrocutaneous syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
4579831016	Oculocerebrocutaneous syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core