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763745005: Intellectual disability Wolff type (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jul 2018. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3643606013 Intellectual disability Wolff type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3643607016 Intellectual disability Wolff type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3643608014 Wolff Zimmermann syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404179019 Intellectual disability, Wolff type is a rare intellectual disability syndrome characterized by severe intellectual disability, characteristic facial features (low anterior hairline, upward slanting palpebral fissures, ocular hypertelorism, broad, bulbous nose, large ears with helix incompletely developed, thick lips, and micrognathia) and additional anomalies including peripheral joint contractures, delayed skeletal maturation, bilateral cleft lip and palate, strabismus, terminal hypoplasia of fingers, hypospadias, and bilateral inguinal hernias. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404180016 Intellectual disability, Wolff type is a rare intellectual disability syndrome characterised by severe intellectual disability, characteristic facial features (low anterior hairline, upward slanting palpebral fissures, ocular hypertelorism, broad, bulbous nose, large ears with helix incompletely developed, thick lips, and micrognathia) and additional anomalies including peripheral joint contractures, delayed skeletal maturation, bilateral cleft lip and palate, strabismus, terminal hypoplasia of fingers, hypospadias, and bilateral inguinal hernias. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3643606013 Intellectual disability Wolff type en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3643607016 Intellectual disability Wolff type (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3643608014 Wolff Zimmermann syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3643610011 A rare intellectual disability syndrome with manifestations of severe intellectual disability, characteristic facial features (low anterior hairline, upward slanting palpebral fissures, ocular hypertelorism, broad, bulbous nose, large ears with helix incompletely developed, thick lips, and micrognathia) and additional anomalies including peripheral joint contractures, delayed skeletal maturation, bilateral cleft lip and palate, strabismus, terminal hypoplasia of fingers, hypospadias, and bilateral inguinal hernias. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404179019 Intellectual disability, Wolff type is a rare intellectual disability syndrome characterized by severe intellectual disability, characteristic facial features (low anterior hairline, upward slanting palpebral fissures, ocular hypertelorism, broad, bulbous nose, large ears with helix incompletely developed, thick lips, and micrognathia) and additional anomalies including peripheral joint contractures, delayed skeletal maturation, bilateral cleft lip and palate, strabismus, terminal hypoplasia of fingers, hypospadias, and bilateral inguinal hernias. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5404180016 Intellectual disability, Wolff type is a rare intellectual disability syndrome characterised by severe intellectual disability, characteristic facial features (low anterior hairline, upward slanting palpebral fissures, ocular hypertelorism, broad, bulbous nose, large ears with helix incompletely developed, thick lips, and micrognathia) and additional anomalies including peripheral joint contractures, delayed skeletal maturation, bilateral cleft lip and palate, strabismus, terminal hypoplasia of fingers, hypospadias, and bilateral inguinal hernias. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3438541001000110 Intelligenzminderung Typ Wolff de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
872401000172113 déficience intellectuelle type Wolff fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
960221000172118 syndrome de Wolff-Zimmermann fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
872401000172113 déficience intellectuelle type Wolff fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
960221000172118 syndrome de Wolff-Zimmermann fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3438541001000110 Intelligenzminderung Typ Wolff 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
Intellectual disability Wolff type Is a Multiple malformation syndrome with facial defects as major feature true Inferred relationship Existential restriction modifier (core metadata concept)
Intellectual disability Wolff type Is a Intelligenzminderung true Inferred relationship Existential restriction modifier (core metadata concept)
Intellectual disability Wolff type Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 1
Intellectual disability Wolff type Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Intellectual disability Wolff type Finding site Face structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Intellectual disability Wolff type Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Intellectual disability Wolff type Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Intellectual disability Wolff type Interprets Intellectual ability (observable entity) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Intellectual disability Wolff type Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Intellectual disability Wolff type Interprets Adaptation behavior true Inferred relationship Existential restriction modifier (core metadata concept) 3
Intellectual disability Wolff type Has interpretation Impaired (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Component annotation with string value reference set (foundation metadata concept)

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