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367520004: Incontinentia pigmenti syndrome (disorder)

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

Descriptions:

Id Description Lang Type Status Case? Module
492592018 Incontinentia pigmenti syndrome en Synonym Active Entire term case insensitive SNOMED CT core module
777035019 Incontinentia pigmenti syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module
1490800010 IP - Incontinentia pigmenti en Synonym Active Entire term case sensitive SNOMED CT core module
1490801014 Incontinentia pigmenti of Bloch-Sulzberger en Synonym Active Only initial character case insensitive SNOMED CT core module
1490802019 Bloch-Sulzberger syndrome en Synonym Active Entire term case sensitive SNOMED CT core module
2164874016 Bloch-Siemens syndrome en Synonym Active Entire term case sensitive SNOMED CT core module

0 descendants.

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Incontinentia pigmenti syndrome Is a Congenital anomaly of skin false Inferred relationship Existential restriction modifier
Incontinentia pigmenti syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Incontinentia pigmenti syndrome Occurrence Congenital false Inferred relationship Existential restriction modifier
Incontinentia pigmenti syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Incontinentia pigmenti syndrome Is a Multisystem disorder false Inferred relationship Existential restriction modifier
Incontinentia pigmenti syndrome Associated morphology Congenital anomaly false Inferred relationship Existential restriction modifier 1
Incontinentia pigmenti syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 1
Incontinentia pigmenti syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 2
Incontinentia pigmenti syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 2
Incontinentia pigmenti syndrome Finding site Skin structure false Inferred relationship Existential restriction modifier 2
Incontinentia pigmenti syndrome Associated morphology Developmental anomaly false Inferred relationship Existential restriction modifier 1
Incontinentia pigmenti syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 1
Incontinentia pigmenti syndrome Is a X-linked hereditary disease false Inferred relationship Existential restriction modifier
Incontinentia pigmenti syndrome Is a Hereditary disorder of the integument true Inferred relationship Existential restriction modifier
Incontinentia pigmenti syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 1
Incontinentia pigmenti syndrome Associated morphology Morphologically abnormal structure false Inferred relationship Existential restriction modifier 1
Incontinentia pigmenti syndrome Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier
Incontinentia pigmenti syndrome Is a Hereditary disorder of tooth true Inferred relationship Existential restriction modifier
Incontinentia pigmenti syndrome Is a X-linked dominant hereditary disease true Inferred relationship Existential restriction modifier
Incontinentia pigmenti syndrome Is a Ectodermal dysplasia with hair-tooth-nail defects true Inferred relationship Existential restriction modifier
Incontinentia pigmenti syndrome Is a Genetic disorder of nail true Inferred relationship Existential restriction modifier
Incontinentia pigmenti syndrome Finding site Tooth structure true Inferred relationship Existential restriction modifier 2
Incontinentia pigmenti syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 2
Incontinentia pigmenti syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 2
Incontinentia pigmenti syndrome Finding site Ectoderm structure true Inferred relationship Existential restriction modifier 1
Incontinentia pigmenti syndrome Associated morphology Dysplasia true Inferred relationship Existential restriction modifier 1
Incontinentia pigmenti syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 3
Incontinentia pigmenti syndrome Finding site Hair structure true Inferred relationship Existential restriction modifier 3
Incontinentia pigmenti syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 3
Incontinentia pigmenti syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 3
Incontinentia pigmenti syndrome Occurrence Congenital true Inferred relationship Existential restriction modifier 4
Incontinentia pigmenti syndrome Finding site Nail unit structure true Inferred relationship Existential restriction modifier 4
Incontinentia pigmenti syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier 4
Incontinentia pigmenti syndrome Pathological process Pathological developmental process true Inferred relationship Existential restriction modifier 4
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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