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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
105066011 Ectoderm en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
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 Only initial character 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 Only initial character 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 Structure of histogenic layer (body structure) true Inferred relationship Existential restriction modifier (core metadata concept)
Ectoderm structure partie de Entire embryo false Additional relationship (core metadata concept) Existential restriction modifier (core metadata concept)
Inbound Relationships Type Active Source Characteristic Refinability Group
Entire ectoderm Is a True Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept)
Neural tube structure Is a True Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept)
Oculodento-osseous dysplasia - severe type Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Robinson nail dystrophy-deafness syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 5
Ectodermal dysplasia with tooth-nail-sweating defect Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
syndrome dento-oculocutané Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Berlin syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Mohr syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Anonychia with bizarre flexural pigmentation Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 5
Basan syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Johanson-Blizzard syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Odontotrichomelic syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Alopecia, nail dystrophy, ophthalmic complications, thyroid dysfunction, hypohidrosis, ephelides, enteropathy and respiratory tract infections Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 5
Ectodermal dysplasia with nail defect Finding site True Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Kirman syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Ectodermal dysplasia with sweating defect Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Roselli-Gulienetti ectodermal dysplasia Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Pachyonychia congenita syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Ectodermal dysplasia with tooth-nail defects Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Flynn-Aird syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Ectodermal dysplasia with tooth-sweating defect Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Laryngo-onychocutaneous syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Anhidrotic ectodermal dysplasia with immune deficiency (disorder) Finding site True Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Cranioectodermal dysplasia Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Greither type of ectodermal dysplasia (disorder) Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Ectodermal dysplasia with hair-tooth-nail defects Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Hay-Wells syndrome of ectodermal dysplasia (disorder) Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Fried's tooth and nail syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Pachyonychia congenita type III of Schafer-Brunauer Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Hallermann-Streiff syndrome (disorder) Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital ectodermal defect Finding site True Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Senter syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Ectodermal dysplasia, syndactyly and pili torti Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Curly hair, ankyloblepharon, nail dysplasia syndrome Finding site True Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Autosomal dominant hypohidrotic ectodermal dysplasia syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Orofacial-digital syndrome IV Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Trichodental syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Dwarfism, alopecia, pseudoanodontia, cutis laxa Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Ectodermal dysplasia Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Marshall syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
syndrome de Moynahan Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Odonto-onychial dysplasia with alopecia Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 5
Curry-Hall syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
dysplasie dermodentaire Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Odontomicronychial ectodermal dysplasia Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Triphalangeal thumbs with onychodystrophy Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Ectodermal dysplasia with hair-tooth-nail-sweating defect Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Tricho-dento-osseous syndrome (disorder) Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Odonto-onycho-dermal dysplasia (disorder) Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Hidrotic ectodermal dysplasia syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Hypoplastic enamel-onycholysis-hypohidrosis syndrome (disorder) Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Hypohidrosis with neurolabyrinthitis (disorder) Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Salamon's syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Amelogenesis imperfecta, intellectual disability, and epileptic seizures. Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Autosomal recessive hypohidrotic ectodermal dysplasia syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Oral-facial-digital syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Ectodermal dysplasia with hair-tooth defects Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Pachyonychia congenita type II of Jackson-Lawler Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Hypodontia and nail dysgenesis Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 7
Hypohidrotic X-linked ectodermal dysplasia Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Orofacial-digital syndrome III Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 1
Schinzel-Giedion syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Chondroectodermal dysplasia (disorder) Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Hypohidrosis-diabetes insipidus syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Ectodermal dysplasia with hair-nail defect Finding site True Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Ectodermal dysplasia-ocular malformation syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Sandman-Andra syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Alopecia, onychodysplasia, hypohidrosis, deafness ectodermal dysplasia Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Tricho-oculodermovertebral syndrome Finding site True Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Oculodentodigital syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Oculodento-osseous dysplasia - mild type Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Schoepf-Schulz-Passage syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Tricho-onychodental dysplasia Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Ectrodactyly-ectodermal dysplasia-clefting syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 5
Curly hair, ankyloblepharon, nail dysplasia syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Ectodermal dysplasia with hair-nail defect Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Tricho-oculodermovertebral syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Congenital ectodermal dysplasia of face Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Congenital ectodermal dysplasia of face Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Mohr syndrome Finding site True Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 5
Odontotrichomelic syndrome Finding site True Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Orofacial-digital syndrome III Finding site True Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 5
Orofacial-digital syndrome IV Finding site True Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 5
Oral-facial-digital syndrome Finding site True Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
A rare syndromic cerebellar ataxia characterized by hypodontia and sparse hair in combination with cerebellar ataxia and normal intelligence. Imaging demonstrates a cerebellar atrophy. Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
Ameloonychohypohidrotic syndrome (disorder) Finding site True Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Zlotogora Ogur syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 5
Ectodermal dysplasia with natal teeth Turnpenny type (disorder) Finding site True Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Oro-facial digital syndrome type 9 (disorder) Finding site True Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 6
Orofaciodigital syndrome type 11 is an extremely rare, sporadic form of Orofaciodigital syndrome with only a few reported cases, and characterized by facial (blepharophimosis, bulbous nasal tip, broad nasal bridge, downslanting palpebral fissures and low set ears) and skeletal (post-axial polydactyly and fusion of vertebrae) malformations along with severe intellectual disability, deafness and congenital heart defects. Finding site True Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 8
Autosomal recessive palmoplantar keratoderma and congenital alopecia syndrome (disorder) Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 6
Sparse hair with short stature and skin anomaly syndrome Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 5
Lelis syndrome Finding site True Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 3
A rare genetic skin disorder characterized by absence of scalp and body hair and palmoplantar keratoderma, without other hand complications. Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 6
Trichomegaly-retina pigmentary degeneration-dwarfism syndrome, also known as Oliver-McFarlane syndrome, is an extremely rare genetic disorder characterized by hair abnormalities, severe chorioretinal atrophy, hypopituitarism, short stature, and intellectual disability. Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 5
Trichodysplasia with amelogenesis imperfecta syndrome (disorder) Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
This syndrome has characteristics of congenital absence of the teeth and sparse or absent hair. Taurodontia is also present in the majority of cases. The syndrome has been described in less than 15 patients from different families. Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Uncombable hair, retinal pigmentary dystrophy, dental anomaly and brachydactyly syndrome (disorder) Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 2
Acro-dermato-ungual-lacrimal-tooth syndrome (disorder) Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 5
Ectodermal dysplasia with ectrodactyly and macular dystrophy syndrome (disorder) Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 4
Alopecia, contracture, dwarfism, intellectual disability syndrome (disorder) Finding site False Ectoderm structure Inferred relationship Existential restriction modifier (core metadata concept) 7

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Reference Sets

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

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