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774208009: Sebaceous nevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, pigmented nevus syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3728357012 SCALP syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3728362013 Sebaceous nevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, pigmented nevus syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3728363015 Sebaceous naevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, pigmented naevus syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3728364014 Sebaceous nevus, central nervous system malformations, aplasia cutis congenita, limbal dermoid, pigmented nevus syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3728359010 A rare skin disease characterised by the association of sebaceous naevus and aplasia cutis congenita (usually on the scalp and face) in conjunction with limbal dermoid of the eye, a giant congenital melanocytic naevus and variable central nervous system abnormalities including seizures, hydrocephalus, neurocutaneous melanosis, arachnoid cysts, and diffuse unilateral hemisphere enlargement. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3728361018 A rare skin disease characterized by the association of sebaceous nevus and aplasia cutis congenita (usually on the scalp and face) in conjunction with limbal dermoid of the eye, a giant congenital melanocytic nevus and variable central nervous system abnormalities including seizures, hydrocephalus, neurocutaneous melanosis, arachnoid cysts, and diffuse unilateral hemisphere enlargement. 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
SCALP syndrome est un(e) (attribut) aplasia cutis congenita (trouble) true Inferred relationship Some
SCALP syndrome morphologie associée (attribut) Epidermal nevus true Inferred relationship Some 3
SCALP syndrome localisation d'une constatation (attribut) structure de la peau true Inferred relationship Some 3
SCALP syndrome survenue (attribut) congénital true Inferred relationship Some 2
SCALP syndrome est un(e) (attribut) Congenital anomaly of central nervous system true Inferred relationship Some
SCALP syndrome est un(e) (attribut) Nevus sebaceous (disorder) true Inferred relationship Some
SCALP syndrome survenue (attribut) congénital true Inferred relationship Some 1
SCALP syndrome est un(e) (attribut) Congenital hamartoma of skin (disorder) true Inferred relationship Some
SCALP syndrome morphologie associée (attribut) Congenital absence false Inferred relationship Some 2
SCALP syndrome localisation d'une constatation (attribut) Structure of central nervous system (body structure) true Inferred relationship Some 1
SCALP syndrome Pathological process (attribute) Pathological developmental process false Inferred relationship Some 3
SCALP syndrome morphologie associée (attribut) structure anormale sur le plan morphologique true Inferred relationship Some 1
SCALP syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
SCALP syndrome survenue (attribut) congénital true Inferred relationship Some 3
SCALP syndrome localisation d'une constatation (attribut) Skin part true Inferred relationship Some 2
SCALP syndrome est un(e) (attribut) syndrome de malformations multisystémiques true Inferred relationship Some
SCALP syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
SCALP syndrome morphologie associée (attribut) Aplasia true Inferred relationship Some 2

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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