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Marfan syndrome type 2

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ORPHA:284973

Classification level: Subtype of disorder

Synonym(s):
  • MFS2

Prevalence: -

Inheritance: Autosomal dominant

Age of onset: All ages

ICD-10: Q87.4

ICD-11: LD28.01

OMIM: 610168

UMLS: C2931058

Summary

This disease is described under Marfan syndrome

Detailed information

Logo ERN: produced/endorsed by ERN(s) Logo FSMR: produced/endorsed by FSMR(s)

General public
Article for general public
Svenska (2017) - Socialstyrelsen
Guidelines
Emergency guidelines
Français (2017.pdf) - Orphanet Urgences
Polski (2007.pdf) - Orphanet Urgences
Deutsch (2014.pdf) - Orphanet Urgences
English (2007.pdf) - Orphanet Urgences
Español (2007.pdf) - Orphanet Urgences
Italiano (2007.pdf) - Orphanet Urgences
Português (2007.pdf) - Orphanet Urgences
Anesthesia guidelines
English (2013) - Orphananesthesia
Español (2013) - Orphananesthesia
Čeština (2013) - Orphananesthesia
Clinical practice guidelines
Français (2018) - PNDS Logo FSMR
English (2024) - Eur Heart J Logo ERN
English (2024) - Eur Heart J Logo ERN
English (2023) - Eur J Med Genet Logo ERN
Disease review articles
Review article
English (2019) - Genet Med
Additional information

Further information on this disease

Patient-centred resources for this disease

Research activities on this disease

Newborn screening

The documents contained in this website are presented for information purposes only. The material is in no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.