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719205008: Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome (disorder)


Status: current, Primitive. Date: 31-Jan 2017. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3315412014 Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3315413016 Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome en Synonym Active Case insensitive SNOMED CT core
3315414010 This syndrome has manifestations of the association of spondylometaphyseal dysplasia (marked by platyspondyly, shortening of the tubular bones and progressive metaphyseal irregularity and cupping), with postnatal growth retardation and progressive visual impairment due to cone-rod dystrophy. So far, it has been described in eight individuals. Transmission appears to be autosomal recessive. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Pathological process Pathological developmental process true Inferred relationship Some 1
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Pathological process Pathological developmental process true Inferred relationship Some 2
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Finding site Bone structure true Inferred relationship Some 2
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Occurrence Congenital true Inferred relationship Some 2
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Associated morphology Dystrophy true Inferred relationship Some 1
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Associated morphology Congenital dysplasia false Inferred relationship Some 2
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Finding site Retinal structure false Inferred relationship Some 1
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Associated morphology Dysplasia true Inferred relationship Some 2
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Is a Spondylometaphyseal dysplasia true Inferred relationship Some
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Is a Congenital anomaly of skeletal bone true Inferred relationship Some
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Clinical course Progressive true Inferred relationship Some 3
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Finding site Neuroepithelial layer true Inferred relationship Some 1
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Is a Chronic disease of musculoskeletal system true Inferred relationship Some
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Is a Hereditary degenerative disease of central nervous system true Inferred relationship Some
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Is a Chronic nervous system disorder true Inferred relationship Some
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Is a Hereditary retinal dystrophy true Inferred relationship Some
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Is a Disorder of visual pathways true Inferred relationship Some
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Is a Metaphyseal chondrodysplasia false Inferred relationship Some
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Is a Progressive cone-rod dystrophy false Inferred relationship Some
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Is a Inherited disorder of connective tissue false Inferred relationship Some
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Is a Hereditary disorder of musculoskeletal system false Inferred relationship Some
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Associated morphology Dystrophy false Inferred relationship Some 3
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Finding site Retinal structure false Inferred relationship Some 3
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Associated morphology Congenital dysplasia false Inferred relationship Some 4
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Occurrence Congenital false Inferred relationship Some 4
Spondylometaphyseal dysplasia with cone-rod dystrophy syndrome Finding site Bone structure false Inferred relationship Some 4

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Musculoskeletal finding reference set

Problem/Diagnosis reference set

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