63206006: Ectoderm structure (body structure)

SNOMED CT Concept\Body structure\Anatomical or acquired body structure\Anatomical structure\...

\Developmental body structure\Embryonic structure\Structure of embryo proper\Early differentiated embryonic structure\Structure of histogenic layer\Ectoderm structure

\Structure of product of conception\Embryonic structure\Structure of embryo proper\Early differentiated embryonic structure\Structure of histogenic layer\Ectoderm structure

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

105066011 Ectoderm en Synonym Active Entire term case insensitive SNOMED CT core module
105067019 Ectoderm, NOS en Synonym Inactive Only initial character case insensitive SNOMED CT core module
499504012 Ectoderm structure en Synonym Active Entire term case insensitive SNOMED CT core module
802464016 Ectoderm structure (body structure) en Fully specified name Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Ectoderm structure	Is a	Structure of histogenic layer	true	Inferred relationship	Existential restriction modifier
Ectoderm structure	Part of	Entire embryo	false	Additional relationship	Existential restriction modifier

Inbound Relationships	Type	Active	Source	Characteristic	Refinability	Group
Revesz syndrome	Finding site	True	Ectoderm structure	Inferred relationship	Existential restriction modifier	11
Focal facial dermal dysplasia	Finding site	True	Ectoderm structure	Inferred relationship	Existential restriction modifier	1
Focal facial dermal dysplasia type I	Finding site	True	Ectoderm structure	Inferred relationship	Existential restriction modifier	1
Focal facial dermal dysplasia type II	Finding site	True	Ectoderm structure	Inferred relationship	Existential restriction modifier	1
Focal facial dermal dysplasia type III	Finding site	True	Ectoderm structure	Inferred relationship	Existential restriction modifier	1
Focal facial dermal dysplasia type IV	Finding site	True	Ectoderm structure	Inferred relationship	Existential restriction modifier	1
Keratitis ichthyosis and deafness syndrome	Finding site	True	Ectoderm structure	Inferred relationship	Existential restriction modifier	5
Autosomal recessive keratitis-ichthyosis-deafness syndrome	Finding site	True	Ectoderm structure	Inferred relationship	Existential restriction modifier	4
Barber-Say syndrome	Finding site	True	Ectoderm structure	Inferred relationship	Existential restriction modifier	2
Onycho-tricho-dysplasia neutropenia syndrome	Finding site	True	Ectoderm structure	Inferred relationship	Existential restriction modifier	1
Sabinas brittle hair syndrome	Finding site	True	Ectoderm structure	Inferred relationship	Existential restriction modifier	1
Incontinentia pigmenti syndrome	Finding site	True	Ectoderm structure	Inferred relationship	Existential restriction modifier	1
Oral-facial-digital syndrome with short stature and brachymesophalangia	Finding site	True	Ectoderm structure	Inferred relationship	Existential restriction modifier	2
Autosomal dominant deafness with onychodystrophy syndrome	Finding site	True	Ectoderm structure	Inferred relationship	Existential restriction modifier	1
Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies	Finding site	True	Ectoderm structure	Inferred relationship	Existential restriction modifier	1
Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome	Finding site	True	Ectoderm structure	Inferred relationship	Existential restriction modifier	3
Pigmentation defects, palmoplantar keratoderma, skin carcinoma syndrome	Finding site	True	Ectoderm structure	Inferred relationship	Existential restriction modifier	1

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This concept is not in any reference sets