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403766000: Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder)

Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2003. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
1771692017 Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1782776012 Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1787861015 Rosenthal-Klöpfer syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
1771692017 Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1771692017 Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
1782776012 Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1782776012 Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
1787861015 Rosenthal-Klöpfer syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
1787861015 Rosenthal-Klöpfer syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
610281000274113 Akromegalie-Cutis verticis gyrata-Kornea-Leukom-Syndrom de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5264401000241111 phénotype acromégaloïde avec cutis verticis gyrata et leucome cornéen fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
5264401000241111 phénotype acromégaloïde avec cutis verticis gyrata et leucome cornéen fr Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
610281000274113 Akromegalie-Cutis verticis gyrata-Kornea-Leukom-Syndrom 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
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Is a Multiple congenital malformations false Inferred relationship Existential restriction modifier (core metadata concept)
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept)
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Associated morphology Congenital malformation false Inferred relationship Existential restriction modifier (core metadata concept)
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Is a Congenital malformation syndrome true Inferred relationship Existential restriction modifier (core metadata concept)
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Is a Corneal leukoma (disorder) false Inferred relationship Existential restriction modifier (core metadata concept)
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Finding site Skin of scalp true Inferred relationship Existential restriction modifier (core metadata concept) 2
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Finding site Corneal structure true Inferred relationship Existential restriction modifier (core metadata concept) 3
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Is a Cutis verticis gyrata true Inferred relationship Existential restriction modifier (core metadata concept)
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Associated morphology Opacity false Inferred relationship Existential restriction modifier (core metadata concept) 3
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Associated morphology dégénérescence false Inferred relationship Existential restriction modifier (core metadata concept) 2
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Is a Congenital sclerocornea false Inferred relationship Existential restriction modifier (core metadata concept)
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Associated morphology Opacity true Inferred relationship Existential restriction modifier (core metadata concept) 1
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Finding site Corneal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Is a Congenital anomaly of skin (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Is a Congenital corneal opacity false Inferred relationship Existential restriction modifier (core metadata concept)
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Associated morphology Degenerative abnormality (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Is a Congenital corneal leucoma true Inferred relationship Existential restriction modifier (core metadata concept)
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Associated morphology Scar (morphologic abnormality) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Acromegaloid phenotype with cutis verticis gyrata and corneal leukoma (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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