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

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Cerebellar ataxia co-occurrent with ectodermal dysplasia

\Finding related to coordination / incoordination\Ataxia\...

\Hereditary ataxia\Cerebellar ataxia co-occurrent with ectodermal dysplasia

\Cerebellar ataxia\Cerebellar ataxia co-occurrent with ectodermal dysplasia

\General finding of soft tissue\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Cerebellar ataxia co-occurrent with ectodermal dysplasia

\Central nervous system finding\Finding of brain\Disorder of brain\Cerebellar disorder\Cerebellar ataxia\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Central nervous system finding\Disorder of the central nervous system\Disorder of brain\Cerebellar disorder\Cerebellar ataxia\Cerebellar ataxia co-occurrent with ectodermal dysplasia

\Finding of head and neck region\Head finding\...

\Finding of brain\Disorder of brain\Cerebellar disorder\Cerebellar ataxia\Cerebellar ataxia co-occurrent with ectodermal dysplasia

\Disorder of head\Disorder of brain\Cerebellar disorder\Cerebellar ataxia\Cerebellar ataxia co-occurrent with ectodermal dysplasia

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Integumentary system finding\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Integumentary system finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Cerebellar ataxia co-occurrent with ectodermal dysplasia

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary ataxia\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal recessive hereditary disorder\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Disease\Disorder of embryonic structure\Congenital ectodermal defect\Ectodermal dysplasia\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of nervous system\Hereditary ataxia\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Disease\Disorder of body system\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Disease\Disorder of body system\Disorder of nervous system\Hereditary disorder of nervous system\Hereditary ataxia\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Disease\Disorder of body system\Disorder of nervous system\Disorder of the central nervous system\Disorder of brain\Cerebellar disorder\Cerebellar ataxia\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Disease\Disorder of head\Disorder of brain\Cerebellar disorder\Cerebellar ataxia\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Disease\Congenital disease\Congenital malformation\Congenital ectodermal defect\Ectodermal dysplasia\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Disease\Developmental disorder\Developmental hereditary disorder\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Disease\Developmental disorder\Congenital malformation\Congenital ectodermal defect\Ectodermal dysplasia\Cerebellar ataxia co-occurrent with ectodermal dysplasia
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Cerebellar ataxia co-occurrent with ectodermal dysplasia

Status: current, Not sufficiently defined by necessary conditions definition status. Date: 31-Jul 2016. Module: SNOMED CT core module

Descriptions:

Id Description Lang Type Status Case? Module

3302385016 Cerebellar ataxia co-occurrent with ectodermal dysplasia (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3302386015 Cerebellar ataxia co-occurrent with ectodermal dysplasia en Synonym Active Entire term case insensitive SNOMED CT core module

3302387012 Cerebellar ataxia and ectodermal dysplasia en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

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

Inbound Relationships

Type

Active

Source

Characteristic

Refinability

Group

This concept is not in any reference sets

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Id	Description	Lang	Type	Status	Case?	Module
3302385016	Cerebellar ataxia co-occurrent with ectodermal dysplasia (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3302386015	Cerebellar ataxia co-occurrent with ectodermal dysplasia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3302387012	Cerebellar ataxia and ectodermal dysplasia	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module