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874931001: Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 31-Jan 2021. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3983331015 Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) en Fully specified name Active Entire term case insensitive (core metadata concept) SNOMED CT core
3983332010 Severe achondroplasia, developmental delay, acanthosis nigricans syndrome en Synonym (core metadata concept) Active Entire term case insensitive (core metadata concept) SNOMED CT core
3983333017 SADDAN (severe achondroplasia, developmental delay, acanthosis nigricans) syndrome en Synonym (core metadata concept) Active Entire term case sensitive (core metadata concept) SNOMED CT core
5408876015 Severe achondroplasia-developmental delay-acanthosis nigricans syndrome is characterized by the association of severe achondroplasia with developmental delay and acanthosis nigricans. It has been described in four unrelated individuals. Structural central nervous system anomalies, seizures and hearing loss were also reported, together with bowing of the clavicle, femur, tibia and fibula in some cases. The syndrome is caused by a Lys650Met substitution in the kinase domain of fibroblast growth factor receptor 3 (encoded by the FGFR3 gene; 4p16.3). en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core
5408877012 Severe achondroplasia-developmental delay-acanthosis nigricans syndrome is characterised by the association of severe achondroplasia with developmental delay and acanthosis nigricans. It has been described in four unrelated individuals. Structural central nervous system anomalies, seizures and hearing loss were also reported, together with bowing of the clavicle, femur, tibia and fibula in some cases. The syndrome is caused by a Lys650Met substitution in the kinase domain of fibroblast growth factor receptor 3 (encoded by the FGFR3 gene; 4p16.3). 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
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Is a Achondroplasia true Inferred relationship Some
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Is a Developmental delay true Inferred relationship Some
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Is a Functional finding false Inferred relationship Some
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Is a Acanthosis nigricans (disorder) true Inferred relationship Some
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Has interpretation Abnormal true Inferred relationship Some 1
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Interprets Keratinization true Inferred relationship Some 1
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Finding site Structure of integumentary system (body structure) true Inferred relationship Some 2
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Occurrence Congenital true Inferred relationship Some 3
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Associated morphology Dysplasia true Inferred relationship Some 3
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Finding site Bone structure true Inferred relationship Some 3
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Finding site Structure of epiphysis true Inferred relationship Some 4
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Occurrence Congenital true Inferred relationship Some 4
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Pathological process (attribute) Pathological developmental process true Inferred relationship Some 4
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Occurrence Congenital true Inferred relationship Some 2
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Is a Hereditary disorder of the integument true Inferred relationship Some
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Associated morphology Hypoplasia true Inferred relationship Some 4
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Interprets Height / growth measure true Inferred relationship Some 5
Severe achondroplasia, developmental delay, acanthosis nigricans syndrome (disorder) Is a Disorder involving the integument of fetus OR newborn 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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US English

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