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715371006: Cerebellar ataxia co-occurrent with ectodermal dysplasia (disorder)


Status: current, Primitive. Date: 31-Jul 2016. Module: SNOMED CT core

Descriptions:

Id Description Lang Type Status Case? Module
3302385016 Cerebellar ataxia co-occurrent with ectodermal dysplasia (disorder) en Fully specified name Active Case insensitive SNOMED CT core
3302386015 Cerebellar ataxia co-occurrent with ectodermal dysplasia en Synonym Active Case insensitive SNOMED CT core
3302387012 Cerebellar ataxia and ectodermal dysplasia en Synonym Active Case insensitive SNOMED CT core
3302388019 A very rare disease, characterized by hypodontia and sparse hair in combination with cerebellar ataxia and normal intelligence. Imaging demonstrates cerebellar atrophy. en Definition Active Case sensitive SNOMED CT core
3302389010 A very rare disease, characterised by hypodontia and sparse hair in combination with cerebellar ataxia and normal intelligence. Imaging demonstrates cerebellar atrophy. en Definition Active Case sensitive SNOMED CT core


0 descendants.

Expanded Value Set


Outbound Relationships Type Target Active Characteristic Refinability Group Values
Cerebellar ataxia and ectodermal dysplasia Occurrence Congenital true Inferred relationship Some 1
Cerebellar ataxia and ectodermal dysplasia Pathological process Pathological developmental process true Inferred relationship Some 1
Cerebellar ataxia and ectodermal dysplasia Pathological process Pathological developmental process true Inferred relationship Some 2
Cerebellar ataxia and ectodermal dysplasia Pathological process Pathological developmental process true Inferred relationship Some 3
Cerebellar ataxia and ectodermal dysplasia Finding site Skin structure true Inferred relationship Some 1
Cerebellar ataxia and ectodermal dysplasia Associated morphology Morphologically abnormal structure true Inferred relationship Some 1
Cerebellar ataxia and ectodermal dysplasia Occurrence Congenital true Inferred relationship Some 2
Cerebellar ataxia and ectodermal dysplasia Finding site Ectoderm structure true Inferred relationship Some 2
Cerebellar ataxia and ectodermal dysplasia Associated morphology Congenital dysplasia false Inferred relationship Some 2
Cerebellar ataxia and ectodermal dysplasia Finding site Cerebellar structure true Inferred relationship Some 3
Cerebellar ataxia and ectodermal dysplasia Associated morphology Dysplasia true Inferred relationship Some 2
Cerebellar ataxia and ectodermal dysplasia Is a Developmental hereditary disorder true Inferred relationship Some
Cerebellar ataxia and ectodermal dysplasia Is a Ectodermal dysplasia true Inferred relationship Some
Cerebellar ataxia and ectodermal dysplasia Is a Cerebellar ataxia true Inferred relationship Some
Cerebellar ataxia and ectodermal dysplasia Is a Autosomal recessive hereditary disorder true Inferred relationship Some
Cerebellar ataxia and ectodermal dysplasia Is a Hereditary disorder of the integument true Inferred relationship Some
Cerebellar ataxia and ectodermal dysplasia Is a Hereditary disorder of nervous system false Inferred relationship Some
Cerebellar ataxia and ectodermal dysplasia Finding site Cerebellar structure false Inferred relationship Some
Cerebellar ataxia and ectodermal dysplasia Occurrence Congenital false Inferred relationship Some 3
Cerebellar ataxia and ectodermal dysplasia Occurrence Congenital false Inferred relationship Some 4
Cerebellar ataxia and ectodermal dysplasia Associated morphology Congenital dysplasia false Inferred relationship Some 3
Cerebellar ataxia and ectodermal dysplasia Finding site Ectoderm structure false Inferred relationship Some 3
Cerebellar ataxia and ectodermal dysplasia Associated morphology Developmental abnormality false Inferred relationship Some 4
Cerebellar ataxia and ectodermal dysplasia Finding site Skin structure false Inferred relationship Some 4
Cerebellar ataxia and ectodermal dysplasia Is a Hereditary ataxia true Inferred relationship Some

Inbound Relationships Type Active Source Characteristic Refinability Group

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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