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720861000: Ehlers-Danlos syndrome progeroid type (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
3322329017 Ehlers-Danlos syndrome progeroid type (disorder) en Fully specified name Active Entire term case sensitive (core metadata concept) SNOMED CT core
3322330010 Ehlers-Danlos syndrome progeroid type en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3322331014 Defective biosynthesis of proteodermatan sulfate en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3322332019 Defective biosynthesis of proteodermatan sulphate en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3322333012 Galactosyltransferase I deficiency en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3322334018 Xylosylprotein 4-beta-galactosyltransferase deficiency en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
4575313016 B4GALT7-related spondylodysplastic EDS (Ehlers-Danlos syndrome) en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402514013 A form of spondylodysplastic Ehlers-Danlos syndrome due to variants in B4GALT7 and characterized by short stature, variable degrees of muscle hypotonia, joint hypermobility, especially of the hands, and bowing of limbs. Additional features include the typical craniofacial gestalt (mid-face hypoplasia, round, flat face, proptosis and narrow mouth), hyperextensible skin that is soft, thin, translucent and doughy, delayed motor and/or cognitive development, characteristic radiographic findings (such as radio-ulnar synostosis, radial head subluxation or dislocation, metaphyseal flaring and osteopenia) and ocular abnormalities. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5402515014 A form of spondylodysplastic Ehlers-Danlos syndrome due to variants in B4GALT7 and characterised by short stature, variable degrees of muscle hypotonia, joint hypermobility, especially of the hands, and bowing of limbs. Additional features include the typical craniofacial gestalt (mid-face hypoplasia, round, flat face, proptosis and narrow mouth), hyperextensible skin that is soft, thin, translucent and doughy, delayed motor and/or cognitive development, characteristic radiographic findings (such as radio-ulnar synostosis, radial head subluxation or dislocation, metaphyseal flaring and osteopenia) and ocular abnormalities. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Ehlers-Danlos syndrome progeroid type (disorder) Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Ehlers-Danlos syndrome progeroid type (disorder) Is a Dysplasia with increased bone density (disorder) true Inferred relationship Some
Ehlers-Danlos syndrome progeroid type (disorder) Is a Ehlers-Danlos syndrome (disorder) false Inferred relationship Some
Ehlers-Danlos syndrome progeroid type (disorder) Is a Premature aging syndrome (disorder) true Inferred relationship Some
Ehlers-Danlos syndrome progeroid type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 3
Ehlers-Danlos syndrome progeroid type (disorder) Occurrence Congenital true Inferred relationship Some 3
Ehlers-Danlos syndrome progeroid type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 4
Ehlers-Danlos syndrome progeroid type (disorder) Occurrence Congenital false Inferred relationship Some 4
Ehlers-Danlos syndrome progeroid type (disorder) Finding site Skin structure false Inferred relationship Some 3
Ehlers-Danlos syndrome progeroid type (disorder) Finding site Bone structure false Inferred relationship Some 4
Ehlers-Danlos syndrome progeroid type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 1
Ehlers-Danlos syndrome progeroid type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Ehlers-Danlos syndrome progeroid type (disorder) Occurrence Congenital true Inferred relationship Some 2
Ehlers-Danlos syndrome progeroid type (disorder) Occurrence Congenital true Inferred relationship Some 1
Ehlers-Danlos syndrome progeroid type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Ehlers-Danlos syndrome progeroid type (disorder) Associated morphology Congenital dysplasia false Inferred relationship Some 2
Ehlers-Danlos syndrome progeroid type (disorder) Finding site Skin structure true Inferred relationship Some 2
Ehlers-Danlos syndrome progeroid type (disorder) Finding site Bone structure true Inferred relationship Some 1
Ehlers-Danlos syndrome progeroid type (disorder) Is a Connective tissue hereditary disorder (disorder) false Inferred relationship Some
Ehlers-Danlos syndrome progeroid type (disorder) Is a Hereditary disorder of musculoskeletal system false Inferred relationship Some
Ehlers-Danlos syndrome progeroid type (disorder) Finding site Connective tissue structure true Inferred relationship Some 3
Ehlers-Danlos syndrome progeroid type (disorder) Associated morphology Dysplasia true Inferred relationship Some 1
Ehlers-Danlos syndrome progeroid type (disorder) Associated morphology Dysplasia true Inferred relationship Some 2
Ehlers-Danlos syndrome progeroid type (disorder) Has interpretation Above reference range true Inferred relationship Some 4
Ehlers-Danlos syndrome progeroid type (disorder) Interprets Bone density scan true Inferred relationship Some 4
Ehlers-Danlos syndrome progeroid type (disorder) Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Ehlers-Danlos syndrome progeroid type (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Ehlers-Danlos syndrome progeroid type (disorder) Is a Spondylodysplastic Ehlers-Danlos syndrome true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

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

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