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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 Is a Aplasia cutis congenita true Inferred relationship Some
SCALP syndrome Associated morphology Epidermal nevus true Inferred relationship Some 3
SCALP syndrome Finding site Skin structure true Inferred relationship Some 3
SCALP syndrome Occurrence Congenital true Inferred relationship Some 2
SCALP syndrome Is a Congenital anomaly of central nervous system true Inferred relationship Some
SCALP syndrome Is a Nevus sebaceous (disorder) true Inferred relationship Some
SCALP syndrome Occurrence Congenital true Inferred relationship Some 1
SCALP syndrome Is a Congenital hamartoma of skin (disorder) true Inferred relationship Some
SCALP syndrome Associated morphology Congenital absence (morphologic abnormality) false Inferred relationship Some 2
SCALP syndrome Finding site 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 Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 1
SCALP syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
SCALP syndrome Occurrence Congenital true Inferred relationship Some 3
SCALP syndrome Finding site Skin part true Inferred relationship Some 2
SCALP syndrome Is a Multiple system malformation syndrome true Inferred relationship Some
SCALP syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
SCALP syndrome Associated morphology 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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