715404000: Ameloonychohypohidrotic syndrome (disorder)

SNOMED CT Concept\Clinical finding\...

\Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Ameloonychohypohidrotic syndrome

\General finding of soft tissue\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Ameloonychohypohidrotic syndrome
\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\Ameloonychohypohidrotic syndrome

\Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Ameloonychohypohidrotic syndrome
\Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Ameloonychohypohidrotic syndrome
\Integumentary system finding\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Ameloonychohypohidrotic syndrome
\Integumentary system finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Ameloonychohypohidrotic syndrome

\Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Ameloonychohypohidrotic syndrome
\Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Ameloonychohypohidrotic syndrome
\Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Ameloonychohypohidrotic syndrome
\Disease\Disorder of embryonic structure\Congenital ectodermal defect\Ectodermal dysplasia\Ameloonychohypohidrotic syndrome
\Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Ameloonychohypohidrotic syndrome
\Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Ameloonychohypohidrotic syndrome
\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\Ameloonychohypohidrotic syndrome
\Disease\Disorder of body system\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Ameloonychohypohidrotic syndrome
\Disease\Congenital disease\Congenital malformation\Congenital ectodermal defect\Ectodermal dysplasia\Ameloonychohypohidrotic syndrome
\Disease\Congenital disease\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Ameloonychohypohidrotic syndrome
\Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Ameloonychohypohidrotic syndrome
\Disease\Developmental disorder\Developmental hereditary disorder\Ameloonychohypohidrotic syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital ectodermal defect\Ectodermal dysplasia\Ameloonychohypohidrotic syndrome
\Disease\Developmental disorder\Congenital malformation\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Ameloonychohypohidrotic syndrome

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

3302487013 Ameloonychohypohidrotic syndrome (disorder) en Fully specified name Active Entire term case insensitive SNOMED CT core module

3302488015 Ameloonychohypohidrotic syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

3302489011 Amelo-onycho-hypohidrotic syndrome en Synonym Active Entire term case insensitive SNOMED CT core module

Expanded Value Set

Outbound Relationships	Type	Target	Active	Characteristic	Refinability	Group	Values
Ameloonychohypohidrotic syndrome	Is a	Ectodermal dysplasia	true	Inferred relationship	Existential restriction modifier
Ameloonychohypohidrotic syndrome	Is a	Autosomal dominant hereditary disorder	true	Inferred relationship	Existential restriction modifier
Ameloonychohypohidrotic syndrome	Is a	Hereditary disorder of the integument	true	Inferred relationship	Existential restriction modifier
Ameloonychohypohidrotic syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	2
Ameloonychohypohidrotic syndrome	Occurrence	Congenital	false	Inferred relationship	Existential restriction modifier	3
Ameloonychohypohidrotic syndrome	Associated morphology	Congenital dysplasia	false	Inferred relationship	Existential restriction modifier	2
Ameloonychohypohidrotic syndrome	Finding site	Ectoderm structure	true	Inferred relationship	Existential restriction modifier	2
Ameloonychohypohidrotic syndrome	Associated morphology	Developmental anomaly	false	Inferred relationship	Existential restriction modifier	3
Ameloonychohypohidrotic syndrome	Finding site	Skin structure	false	Inferred relationship	Existential restriction modifier	3
Ameloonychohypohidrotic syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	1
Ameloonychohypohidrotic syndrome	Occurrence	Congenital	true	Inferred relationship	Existential restriction modifier	1
Ameloonychohypohidrotic syndrome	Finding site	Skin structure	true	Inferred relationship	Existential restriction modifier	1
Ameloonychohypohidrotic syndrome	Associated morphology	Morphologically abnormal structure	true	Inferred relationship	Existential restriction modifier	1
Ameloonychohypohidrotic syndrome	Pathological process	Pathological developmental process	true	Inferred relationship	Existential restriction modifier	2
Ameloonychohypohidrotic syndrome	Associated morphology	Dysplasia	true	Inferred relationship	Existential restriction modifier	2
Ameloonychohypohidrotic syndrome	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

Back to Start

Id	Description	Lang	Type	Status	Case?	Module
3302487013	Ameloonychohypohidrotic syndrome (disorder)	en	Fully specified name	Active	Entire term case insensitive	SNOMED CT core module
3302488015	Ameloonychohypohidrotic syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module
3302489011	Amelo-onycho-hypohidrotic syndrome	en	Synonym	Active	Entire term case insensitive	SNOMED CT core module