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\Amelo-onycho-hypohidrotic syndrome
• \General finding of soft tissue\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Amelo-onycho-hypohidrotic 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\Amelo-onycho-hypohidrotic syndrome
• \Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Amelo-onycho-hypohidrotic syndrome
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Amelo-onycho-hypohidrotic syndrome
• \Integumentary system finding\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Amelo-onycho-hypohidrotic syndrome
• \Integumentary system finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Amelo-onycho-hypohidrotic syndrome
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Amelo-onycho-hypohidrotic syndrome
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Amelo-onycho-hypohidrotic syndrome
• \Disease\Genetic disease\Hereditary disease\Autosomal hereditary disorder\Autosomal dominant hereditary disorder\Amelo-onycho-hypohidrotic syndrome
• \Disease\Disorder of embryonic structure\Congenital ectodermal defect\Ectodermal dysplasia\Amelo-onycho-hypohidrotic syndrome
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Amelo-onycho-hypohidrotic syndrome
• \Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Amelo-onycho-hypohidrotic 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\Amelo-onycho-hypohidrotic syndrome
• \Disease\Disorder of body system\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Amelo-onycho-hypohidrotic syndrome
• \Disease\Congenital disease\Congenital anomaly\Congenital ectodermal defect\Ectodermal dysplasia\Amelo-onycho-hypohidrotic syndrome
• \Disease\Congenital disease\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Amelo-onycho-hypohidrotic syndrome
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Amelo-onycho-hypohidrotic syndrome
• \Disease\Developmental disorder\Developmental hereditary disorder\Amelo-onycho-hypohidrotic syndrome
• \Disease\Developmental disorder\Congenital anomaly\Congenital ectodermal defect\Ectodermal dysplasia\Amelo-onycho-hypohidrotic syndrome
• \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Genodermatosis\Ectodermal dysplasia\Amelo-onycho-hypohidrotic syndrome

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

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3302487013	Ameloonychohypohidrotic syndrome (disorder)	en	Fully specified name	Active	Case insensitive	SNOMED CT core
3302488015	Ameloonychohypohidrotic syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
3302489011	Amelo-onycho-hypohidrotic syndrome	en	Synonym	Active	Case insensitive	SNOMED CT core
3302490019	A rare syndrome comprising hypocalcified-hypoplastic tooth enamel, onycholysis with subungual hyperkeratosis, and hypohidrosis.	en	Definition	Active	Case sensitive	SNOMED CT core

Expanded Value Set

Reference Sets

Australian emergency department reference set

Clinical finding foundation reference set

Problem/Diagnosis reference set

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