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367520004: Incontinentia pigmenti syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
492592018 Incontinentia pigmenti syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
777035019 Incontinentia pigmenti syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1490800010 IP - Incontinentia pigmenti en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1490801014 Incontinentia pigmenti of Bloch-Sulzberger en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1490802019 Bloch-Sulzberger syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2164874016 Bloch-Siemens syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
492592018 Incontinentia pigmenti syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
492592018 Incontinentia pigmenti syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
492593011 Ito's syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
492594017 Incontinentia pigmenti achromians syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
777035019 Incontinentia pigmenti syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
777035019 Incontinentia pigmenti syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1490799011 Bloch-Siemans syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1490800010 IP - Incontinentia pigmenti en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1490801014 Incontinentia pigmenti of Bloch-Sulzberger en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1490802019 Bloch-Sulzberger syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
2164874016 Bloch-Siemens syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
2164874016 Bloch-Siemens syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3430741001000118 Incontinentia pigmenti de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
147021000077110 incontinentia pigmenti fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
147021000077110 incontinentia pigmenti fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3430741001000118 Incontinentia pigmenti de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Incontinentia pigmenti syndrome Is a Congenital anomaly of skin (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Incontinentia pigmenti syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Incontinentia pigmenti syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Incontinentia pigmenti syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Incontinentia pigmenti syndrome Is a trouble multisytémique false Inferred relationship Existential restriction modifier (core metadata concept)
Incontinentia pigmenti syndrome Associated morphology anomalie congénitale false Inferred relationship Existential restriction modifier (core metadata concept) 1
Incontinentia pigmenti syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Incontinentia pigmenti syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Incontinentia pigmenti syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 2
Incontinentia pigmenti syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier (core metadata concept) 2
Incontinentia pigmenti syndrome Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Incontinentia pigmenti syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Incontinentia pigmenti syndrome Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier (core metadata concept)
Incontinentia pigmenti syndrome Is a Hereditary disorder of the integument (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Incontinentia pigmenti syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Incontinentia pigmenti syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier (core metadata concept) 1
Incontinentia pigmenti syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)
Incontinentia pigmenti syndrome Is a Hereditary disorder of tooth true Inferred relationship Existential restriction modifier (core metadata concept)
Incontinentia pigmenti syndrome Is a X-linked dominant hereditary disease (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Incontinentia pigmenti syndrome Is a Ectodermal dysplasia with hair-tooth-nail defects true Inferred relationship Existential restriction modifier (core metadata concept)
Incontinentia pigmenti syndrome Is a Genetic disorder of nail (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Incontinentia pigmenti syndrome Finding site Tooth structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Incontinentia pigmenti syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Incontinentia pigmenti syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Incontinentia pigmenti syndrome Finding site Ectoderm structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Incontinentia pigmenti syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier (core metadata concept) 1
Incontinentia pigmenti syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Incontinentia pigmenti syndrome Finding site Hair structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Incontinentia pigmenti syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Incontinentia pigmenti syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Incontinentia pigmenti syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 4
Incontinentia pigmenti syndrome Finding site Nail unit structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 4
Incontinentia pigmenti syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 4
Incontinentia pigmenti syndrome Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 4

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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