205573006: Focal dermal hypoplasia (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Focal dermal hypoplasia
• \General finding of soft tissue\Skin finding\Disorder of skin\Congenital anomaly of skin\Focal dermal hypoplasia
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Focal dermal hypoplasia
• \Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Focal dermal hypoplasia
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Focal dermal hypoplasia
• \Integumentary system finding\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Focal dermal hypoplasia
• \Integumentary system finding\Skin finding\Disorder of skin\Congenital anomaly of skin\Focal dermal hypoplasia
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Focal dermal hypoplasia
• \Disease\Genetic disease\Hereditary disease\Developmental hereditary disorder\Focal dermal hypoplasia
• \Disease\Genetic disease\Hereditary disease\Sex-linked hereditary disorder\X-linked hereditary disease\X-linked dominant hereditary disease\Focal dermal hypoplasia
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Focal dermal hypoplasia
• \Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Focal dermal hypoplasia
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Focal dermal hypoplasia
• \Disease\Disorder of body system\Disorder of integument\Congenital anomaly of integument\Congenital anomaly of skin\Focal dermal hypoplasia
• \Disease\Congenital disease\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Focal dermal hypoplasia
• \Disease\Congenital disease\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Focal dermal hypoplasia
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Congenital anomaly of skin\Focal dermal hypoplasia
• \Disease\Developmental disorder\Developmental hereditary disorder\Focal dermal hypoplasia
• \Disease\Developmental disorder\Congenital anomaly\Congenital malformation syndrome\Multiple system malformation syndrome\Focal dermal hypoplasia
• \Disease\Developmental disorder\Congenital anomaly\Congenital anomaly of integument\Congenital anomaly of skin\Focal dermal hypoplasia

Status: current, Primitive. Date: 31-Jan 2002. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
315257012	Focal dermal hypoplasia	en	Synonym	Active	Case insensitive	SNOMED CT core
315258019	FDH - Focal dermal hypoplasia	en	Synonym	Active	Case sensitive	SNOMED CT core
315259010	FODH - Focal dermal hypoplasia	en	Synonym	Active	Case sensitive	SNOMED CT core
3781377015	Goltz-Gorlin syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3781378013	Goltz syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
590960012	Focal dermal hypoplasia (disorder)	en	Fully specified name	Active	Case insensitive	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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