FHIR © HL7.org  |  Server Home  |  FHIR Server FHIR Server 3.7.10  |  FHIR Version n/a  User: [n/a]

1251488008: Spondylodysplastic Ehlers-Danlos syndrome (disorder)


Status: current, Not sufficiently defined by necessary conditions definition status (core metadata concept). Date: 30-Sep 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5133782011 Spondylodysplastic Ehlers-Danlos syndrome en Synonym (core metadata concept) Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5133783018 Spondylodysplastic Ehlers-Danlos syndrome (disorder) en Fully specified name Active Only initial character case insensitive (core metadata concept) SNOMED CT core
5133784012 A rare connective tissue disorder for which three subtypes exist, either related to the gene B4GALT7, B3GALT6 or SLC39A13, and for which the clinically overlapping characteristics include short stature (progressive in childhood), small joint hypermobility, skin hyperextensibility with soft, doughy skin especially on the hands and feet, muscular hypotonia (ranging from congenitally severe to mild with later onset), skeletal anomalies and more variably osteopenia, delayed motor development and bowing of the limbs. Gene-specific features with variable presentation are additionally observed in each subtype. en Definition Active Entire term case sensitive (core metadata concept) SNOMED CT core


3 descendants. Search Descendants:

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spondylodysplastic Ehlers-Danlos syndrome Is a Ehlers-Danlos syndrome (disorder) true Inferred relationship Some
Spondylodysplastic Ehlers-Danlos syndrome Occurrence Congenital true Inferred relationship Some 1
Spondylodysplastic Ehlers-Danlos syndrome Finding site Bone structure true Inferred relationship Some 1
Spondylodysplastic Ehlers-Danlos syndrome Associated morphology Dysplasia true Inferred relationship Some 1
Spondylodysplastic Ehlers-Danlos syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 1
Spondylodysplastic Ehlers-Danlos syndrome Occurrence Congenital true Inferred relationship Some 2
Spondylodysplastic Ehlers-Danlos syndrome Finding site Skin structure true Inferred relationship Some 2
Spondylodysplastic Ehlers-Danlos syndrome Associated morphology Dysplasia true Inferred relationship Some 2
Spondylodysplastic Ehlers-Danlos syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 2
Spondylodysplastic Ehlers-Danlos syndrome Occurrence Congenital true Inferred relationship Some 3
Spondylodysplastic Ehlers-Danlos syndrome Finding site Connective tissue structure true Inferred relationship Some 3
Spondylodysplastic Ehlers-Danlos syndrome Associated morphology Morphologically abnormal structure (morphologic abnormality) true Inferred relationship Some 3
Spondylodysplastic Ehlers-Danlos syndrome Pathological process (attribute) Pathological developmental process true Inferred relationship Some 3

Inbound Relationships Type Active Source Characteristic Refinability Group
Ehlers-Danlos syndrome spondylocheirodysplastic type Is a True Spondylodysplastic Ehlers-Danlos syndrome Inferred relationship Some
Ehlers-Danlos syndrome progeroid type (disorder) Is a True Spondylodysplastic Ehlers-Danlos syndrome Inferred relationship Some
Beta-1,3-galactosyltransferase 6-related spondylodysplastic Ehlers-Danlos syndrome (disorder) Is a True Spondylodysplastic Ehlers-Danlos syndrome Inferred relationship Some

This concept is not in any reference sets

Back to Start