770567006: Progeroid syndrome Petty type (disorder)

• SNOMED CT Concept\Clinical finding\...
• \Skin AND/OR mucosa finding\Skin finding\Disorder of skin\Premature ageing syndrome\Progeroid syndrome Petty type
• \General finding of soft tissue\Skin finding\Disorder of skin\Premature ageing syndrome\Progeroid syndrome Petty type
• \General finding of soft tissue\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature ageing syndrome\Progeroid syndrome Petty type
• \Integumentary system finding\Disorder of integument\Hereditary disorder of the integument\Premature ageing syndrome\Progeroid syndrome Petty type
• \Integumentary system finding\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature ageing syndrome\Progeroid syndrome Petty type
• \Integumentary system finding\Skin finding\Disorder of skin\Premature ageing syndrome\Progeroid syndrome Petty type
• \Disease\Genetic disease\Hereditary disease\Hereditary metabolic disease\Inborn error of metabolism\Premature ageing syndrome\Progeroid syndrome Petty type
• \Disease\Genetic disease\Hereditary disease\Hereditary disorder by system\Hereditary disorder of the integument\Premature ageing syndrome\Progeroid syndrome Petty type
• \Disease\Disorder of body system\Hereditary disorder by system\Hereditary disorder of the integument\Premature ageing syndrome\Progeroid syndrome Petty type
• \Disease\Disorder of body system\Disorder of integument\Hereditary disorder of the integument\Premature ageing syndrome\Progeroid syndrome Petty type
• \Disease\Disorder of body system\Disorder of integument\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature ageing syndrome\Progeroid syndrome Petty type
• \Disease\Metabolic disease\Hereditary metabolic disease\Inborn error of metabolism\Premature ageing syndrome\Progeroid syndrome Petty type
• \Disease\Congenital disease\Inborn error of metabolism\Premature ageing syndrome\Progeroid syndrome Petty type
• \Disease\Disorder of soft tissue\Disorder of skin and/or subcutaneous tissue\Disorder of skin\Premature ageing syndrome\Progeroid syndrome Petty type

Status: current, Primitive. Date: 31-Jan 2019. Module: SNOMED CT core

Descriptions:

Id	Description	Lang	Type	Status	Case?	Module
3701302010	Progeroid syndrome Petty type	en	Synonym	Active	Initial character case insensitive	SNOMED CT core
3701303017	Progeroid syndrome Petty type (disorder)	en	Fully specified name	Active	Initial character case insensitive	SNOMED CT core
3701304011	Petty syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3701307016	Petty Laxova Wiedemann syndrome	en	Synonym	Active	Case sensitive	SNOMED CT core
3701306013	A rare premature aging syndrome with characteristics of pre and postnatal growth retardation, a congenital premature-aged appearance with distinctive craniofacial dysmorphism (wide calvaria with large open anterior fontanelle and wide metopic suture, broad forehead, small face, micrognathia), markedly diminished subcutaneous fat, cutis laxa and wrinkled skin, without delay in psychomotor development. Scant, brittle hair, hypoplastic nails and delayed, abnormal dentition, as well as hypoplastic distal phalanges, umbilical hernia and eye abnormalities (myopia/hyperopia, strabismus), are also commonly associated.	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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