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1251499005: Beta-1,3-galactosyltransferase 6-related spondylodysplastic Ehlers-Danlos syndrome (disorder)


Status: current, Primitive. Date: 30-Sep 2022. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
5133834012 Beta-1,3-galactosyltransferase 6-related spondylodysplastic Ehlers-Danlos syndrome en Synonym Active Initial character case insensitive SNOMED CT core
5133835013 Beta-1,3-galactosyltransferase 6-related spondylodysplastic Ehlers-Danlos syndrome (disorder) en Fully specified name Active Initial character case insensitive SNOMED CT core
5133836014 B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome en Synonym Active Case sensitive SNOMED CT core
5133837017 Ehlers-Danlos syndrome progeroid type 2 en Synonym Active Case sensitive SNOMED CT core
5133838010 A form of spondylodysplastic Ehlers-Danlos syndrome due to variants in B3GALT6 with characteristics of short stature, variable degrees of muscle hypotonia, joint hypermobility, especially of the hands, bowing of limbs and congenital or early onset, progressive kyphoscoliosis. Additional features include the typical craniofacial gestalt (prominent forehead, sparse hair, mid-face hypoplasia, blue sclerae, proptosis and abnormal dentition), hyperextensible, soft, thin, translucent and doughy skin, delayed motor and/or cognitive development, characteristic radiographic findings (spondyloepimetaphyseal dysplasia, platyspondyly, anterior beak of vertebral body, short ilia, elbow malalignment and generalised osteoporosis), joint contractures and ascending aortic aneurysm. The disorder is due to variants of the B3GALT6 gene (1p36.33), encoding for galactosyltransferase II. Transmission is autosomal recessive. en Definition Active Case sensitive SNOMED CT core
5133839019 A form of spondylodysplastic Ehlers-Danlos syndrome due to variants in B3GALT6 with characteristics of short stature, variable degrees of muscle hypotonia, joint hypermobility, especially of the hands, bowing of limbs and congenital or early onset, progressive kyphoscoliosis. Additional features include the typical craniofacial gestalt (prominent forehead, sparse hair, mid-face hypoplasia, blue sclerae, proptosis and abnormal dentition), hyperextensible, soft, thin, translucent and doughy skin, delayed motor and/or cognitive development, characteristic radiographic findings (spondyloepimetaphyseal dysplasia, platyspondyly, anterior beak of vertebral body, short ilia, elbow malalignment and generalized osteoporosis), joint contractures and ascending aortic aneurysm. The disorder is due to variants of the B3GALT6 gene (1p36.33), encoding for galactosyltransferase II. Transmission is autosomal recessive. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Is a Spondylodysplastic Ehlers-Danlos syndrome true Inferred relationship Some
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Is a Short stature disorder true Inferred relationship Some
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Is a Kyphoscoliosis deformity of spine true Inferred relationship Some
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Interprets Body height measure true Inferred relationship Some 5
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Has interpretation Below reference range true Inferred relationship Some 5
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Occurrence Congenital true Inferred relationship Some 1
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Finding site Bone structure true Inferred relationship Some 1
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Associated morphology Dysplasia true Inferred relationship Some 1
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Occurrence Congenital true Inferred relationship Some 2
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Finding site Skin structure true Inferred relationship Some 2
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Associated morphology Dysplasia true Inferred relationship Some 2
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Occurrence Congenital true Inferred relationship Some 4
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Finding site Connective tissue structure true Inferred relationship Some 4
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Associated morphology Morphologically abnormal structure true Inferred relationship Some 4
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Pathological process Pathological developmental process true Inferred relationship Some 4
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Finding site Musculoskeletal structure of spine true Inferred relationship Some 3
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Associated morphology Lateral abnormal curvature true Inferred relationship Some 3
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Finding site Musculoskeletal structure of spine true Inferred relationship Some 6
B3GALT6-related spondylodysplastic Ehlers-Danlos syndrome Associated morphology Anteroposterior abnormal curvature true Inferred relationship Some 6

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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