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719256004: Pterygium colli with intellectual disability and digital anomaly syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3315704019 Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3315705018 Pterygium colli with intellectual disability and digital anomaly syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3315706017 Khalifa Graham syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402031012 A rare disorder characterized by pterygium colli, digital anomalies (abnormal small thumbs, widened interphalangeal joints, and broad terminal phalanges), and craniofacial abnormalities (brachycephaly, epicanthic folds, angulated eyebrows, upward slanting of the palpebral fissures, ptosis, hypertelorism, and prominent low-set, posteriorly rotated ears). It has been described in a woman and her son, but the manifestations were much less severe in the mother. The son also had intellectual deficit. The inheritance is either X-linked dominant or autosomal dominant. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402032017 A rare disorder characterised by pterygium colli, digital anomalies (abnormal small thumbs, widened interphalangeal joints, and broad terminal phalanges), and craniofacial abnormalities (brachycephaly, epicanthic folds, angulated eyebrows, upward slanting of the palpebral fissures, ptosis, hypertelorism, and prominent low-set, posteriorly rotated ears). It has been described in a woman and her son, but the manifestations were much less severe in the mother. The son also had intellectual deficit. The inheritance is either X-linked dominant or autosomal dominant. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3315704019 Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3315704019 Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3315705018 Pterygium colli with intellectual disability and digital anomaly syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3315705018 Pterygium colli with intellectual disability and digital anomaly syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3315706017 Khalifa Graham syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3315710019 This syndrome has characteristics of pterygium colli, digital anomalies and craniofacial abnormalities. Digital anomalies include abnormal small thumbs, widened interphalangeal joints, and broad terminal phalanges. Craniofacial abnormalities include brachycephaly, epicanthic folds, angulated eyebrows, upward slanting of the palpebral fissures, ptosis, hypertelorism, prominent low-set and posteriorly rotated ears. It has been described in a woman and her son, but the manifestations were much less severe in the mother. The son also had intellectual deficit. The inheritance is either X-linked dominant or autosomal dominant. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402031012 A rare disorder characterized by pterygium colli, digital anomalies (abnormal small thumbs, widened interphalangeal joints, and broad terminal phalanges), and craniofacial abnormalities (brachycephaly, epicanthic folds, angulated eyebrows, upward slanting of the palpebral fissures, ptosis, hypertelorism, and prominent low-set, posteriorly rotated ears). It has been described in a woman and her son, but the manifestations were much less severe in the mother. The son also had intellectual deficit. The inheritance is either X-linked dominant or autosomal dominant. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402032017 A rare disorder characterised by pterygium colli, digital anomalies (abnormal small thumbs, widened interphalangeal joints, and broad terminal phalanges), and craniofacial abnormalities (brachycephaly, epicanthic folds, angulated eyebrows, upward slanting of the palpebral fissures, ptosis, hypertelorism, and prominent low-set, posteriorly rotated ears). It has been described in a woman and her son, but the manifestations were much less severe in the mother. The son also had intellectual deficit. The inheritance is either X-linked dominant or autosomal dominant. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
3389011001000114 Pterygium colli - Intelligenzminderung - Fingeranomalien de Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT Switzerland NRC maintained Module
3389011001000114 Pterygium colli - Intelligenzminderung - Fingeranomalien 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
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Finding site Face structure (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 3
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Is a Neck webbing (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Is a Multiple malformation syndrome with facial-limb defects as major feature true Inferred relationship Existential restriction modifier (core metadata concept)
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Is a Hereditary disorder of the integument (disorder) true Inferred relationship Existential restriction modifier (core metadata concept)
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Associated morphology Congenital webbing true Inferred relationship Existential restriction modifier (core metadata concept) 3
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 3
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Finding site Skin structure of neck (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 4
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 4
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Finding site Limb structure false Inferred relationship Existential restriction modifier (core metadata concept) 4
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Occurrence Congenital false Inferred relationship Existential restriction modifier (core metadata concept) 5
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Associated morphology anomalie du développement false Inferred relationship Existential restriction modifier (core metadata concept) 3
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Associated morphology Congenital webbing false Inferred relationship Existential restriction modifier (core metadata concept) 5
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Finding site Skin structure of neck (body structure) false Inferred relationship Existential restriction modifier (core metadata concept) 5
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 2
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 3
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Pathological process (attribute) Pathological developmental process (qualifier value) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Occurrence Congenital true Inferred relationship Existential restriction modifier (core metadata concept) 2
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Finding site Face structure (body structure) true Inferred relationship Existential restriction modifier (core metadata concept) 2
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Associated morphology Morphologically abnormal structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Finding site Limb structure true Inferred relationship Existential restriction modifier (core metadata concept) 1
Pterygium colli with intellectual disability and digital anomaly syndrome (disorder) Is a Developmental hereditary disorder true Inferred relationship Existential restriction modifier (core metadata concept)

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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