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63206006: Ectoderm structure (body structure)

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
105066011 Ectoderm en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
499504012 Ectoderm structure en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
802464016 Ectoderm structure (body structure) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core

15 descendants. Search Descendants:

Expanded Value Set

Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ectoderm structure Is a Histogenic layer true Inferred relationship Some
Ectoderm structure Part of Entire embryo false Additional relationship Some
Inbound Relationships Type Active Source Characteristic Refinability Group
Revesz syndrome (disorder) Finding site True Ectoderm structure Inferred relationship Some 11
Focal facial dermal dysplasia (disorder) Finding site True Ectoderm structure Inferred relationship Some 1
Focal facial dermal dysplasia type I Finding site True Ectoderm structure Inferred relationship Some 1
Focal facial dermal dysplasia type II Finding site True Ectoderm structure Inferred relationship Some 1
Focal facial dermal dysplasia type III Finding site True Ectoderm structure Inferred relationship Some 1
Focal facial dermal dysplasia type IV (disorder) Finding site True Ectoderm structure Inferred relationship Some 1
Keratitis ichthyosis and deafness syndrome (disorder) Finding site True Ectoderm structure Inferred relationship Some 5
Autosomal recessive keratitis-ichthyosis-deafness syndrome (disorder) Finding site True Ectoderm structure Inferred relationship Some 4
Barber-Say syndrome (disorder) Finding site True Ectoderm structure Inferred relationship Some 2
Onycho-tricho-dysplasia neutropenia syndrome Finding site True Ectoderm structure Inferred relationship Some 1
Sabinas brittle hair syndrome (disorder) Finding site True Ectoderm structure Inferred relationship Some 1
Incontinentia pigmenti syndrome Finding site True Ectoderm structure Inferred relationship Some 1
Oral-facial-digital syndrome with short stature and brachymesophalangia Finding site True Ectoderm structure Inferred relationship Some 2
Autosomal dominant deafness with onychodystrophy syndrome Finding site True Ectoderm structure Inferred relationship Some 1
Linear hypopigmentation and craniofacial asymmetry with acral, ocular and brain anomalies Finding site True Ectoderm structure Inferred relationship Some 1
Craniofacial dysplasia, short stature, ectodermal anomalies, intellectual disability syndrome (disorder) Finding site True Ectoderm structure Inferred relationship Some 3
Pigmentation defects, palmoplantar keratoderma, skin carcinoma syndrome (disorder) Finding site True Ectoderm structure Inferred relationship Some 1
Ectodermal dysplasia, hyperhidrosis, cutaneous syndactyly syndrome (disorder) Finding site True Ectoderm structure Inferred relationship Some 1
Anhidrotic ectodermal dysplasia with immune deficiency due to IKBA gain of function mutation Finding site True Ectoderm structure Inferred relationship Some 2

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Reference Sets

Anatomy structure and entire association reference set (foundation metadata concept)

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