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778068007: Autosomal recessive cutis laxa type 2B (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3737618018 Autosomal recessive cutis laxa type 2B en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3737619014 Autosomal recessive cutis laxa type 2B (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
3737620015 Autosomal recessive cutis laxa type 2 progeroid type en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3737621016 ARCL2B - autosomal recessive cutis laxa type 2B en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
3737622011 A rare hereditary developmental defect with connective tissue involvement and characteristics of cutis laxa of variable severity, in utero growth restriction, congenital hip dislocation and joint hyperlaxity, wrinkling of the skin, in particular the dorsum of hands and feet and progeroid facial features. Hypotonia, developmental delay, and intellectual disability are common. In addition, cataracts, corneal clouding, wormian bones, lipodystrophy and osteopenia have been reported. There is evidence the disease is caused by homozygous or compound heterozygous mutation in the PYCR1 gene on chromosome 17q25. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
948471000172113 ARCL2 type progéroïde fr Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
978631000172114 cutis laxa autosomique récessive type 2B fr Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)
893661000172113 ARCL2 (autosomaal recessieve cutis laxa), progeroïd type nl Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) Belgian module (core metadata concept)
1001811000172111 autosomaal recessieve cutis laxa type 2B nl Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) Belgian module (core metadata concept)


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Autosomal recessive cutis laxa type 2B Occurrence Congenital true Inferred relationship Some 1
Autosomal recessive cutis laxa type 2B Is a Metabolic bone disease true Inferred relationship Some
Autosomal recessive cutis laxa type 2B Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 2
Autosomal recessive cutis laxa type 2B Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Autosomal recessive cutis laxa type 2B Occurrence Congenital true Inferred relationship Some 2
Autosomal recessive cutis laxa type 2B Finding site Bone structure true Inferred relationship Some 1
Autosomal recessive cutis laxa type 2B Is a Dysplasia with decreased bone density true Inferred relationship Some
Autosomal recessive cutis laxa type 2B Is a Disorder of proline AND/OR hydroxyproline metabolism true Inferred relationship Some
Autosomal recessive cutis laxa type 2B Is a Hereditary disorder of musculoskeletal system true Inferred relationship Some
Autosomal recessive cutis laxa type 2B Is a Cutis laxa, recessive, type II true Inferred relationship Some
Autosomal recessive cutis laxa type 2B Finding site Skin structure true Inferred relationship Some 2
Autosomal recessive cutis laxa type 2B Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Autosomal recessive cutis laxa type 2B Associated morphology Congenital dysplasia false Inferred relationship Some 1
Autosomal recessive cutis laxa type 2B Finding site Connective tissue structure false Inferred relationship Some
Autosomal recessive cutis laxa type 2B Is a Musculoskeletal and connective tissue disorder (disorder) true Inferred relationship Some
Autosomal recessive cutis laxa type 2B Associated morphology Dysplasia true Inferred relationship Some 1
Autosomal recessive cutis laxa type 2B Has interpretation Below reference range true Inferred relationship Some 4
Autosomal recessive cutis laxa type 2B Interprets Bone density scan true Inferred relationship Some 4
Autosomal recessive cutis laxa type 2B Occurrence Congenital true Inferred relationship Some 3
Autosomal recessive cutis laxa type 2B Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Autosomal recessive cutis laxa type 2B Finding site Connective tissue structure true Inferred relationship Some 3
Autosomal recessive cutis laxa type 2B Is a Congenital anomaly of skin true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

This concept is not in any reference sets

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