Fabry disease
Fabry disease, also known as Anderson–Fabry disease, is a rare genetic disease that can affect many parts of the body, including the kidneys, heart, and skin. Fabry disease is one of a group of conditions known as lysosomal storage diseases. The genetic mutation that causes Fabry disease interferes with the function of an enzyme that processes biomolecules known as sphingolipids, leading to these substances building up in the walls of blood vessels and other organs. It is inherited in an X-linked manner.
medical cause
Alpha-galactosidase A deficiencyAnderson-Fabry's DiseaseAnderson-Fabry diseaseAnderson–Fabry diseaseAngiokeratoma Corporis DiffusumAngiokeratoma corporis diffusumAngiokeratoma corporis diffusum of FabryAngiokeratoma corporis diffusum universaleAngiokeratoma diffuseAnglokeratoma corporis diffusum universaleCeramide trihexosidase deficiencyCeramide trihexosidosisDiffuse angiokeratomaDiffuse angiokeratosisDiffuse anglokeratomaFabray's diseaseFabrey's diseaseFabry's DiseaseFabry's diseaseFabrys diseaseGLA (gene)
Wikipage redirect
Albrecht Kossel Institute for NeuroregenerationAlpha-galactosidaseAlpha-galactosidase A deficiencyAnderson-Fabry's DiseaseAnderson-Fabry diseaseAnderson–Fabry diseaseAngiokeratomaAngiokeratoma Corporis DiffusumAngiokeratoma corporis diffusumAngiokeratoma corporis diffusum of FabryAngiokeratoma corporis diffusum universaleAngiokeratoma diffuseAnglokeratoma corporis diffusum universaleAortic stenosisBayh–Dole ActCataractCeramide trihexosidase deficiencyCeramide trihexosidosisCholinergic urticariaCongenital cataractCornea verticillataCoronary flow reserveDavid SillenceDiffuse angiokeratomaDiffuse angiokeratosisDiffuse anglokeratomaDoctor_John_(TV_series)Embolic stroke of undetermined sourceEnzyme replacement therapyEpic Fail (House)ErythromelalgiaFabray's diseaseFabrey's diseaseFabryFabry's DiseaseFabry's diseaseFabrys diseaseFeverFever of unknown originGLA
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primaryTopic
Fabry disease
Fabry disease, also known as Anderson–Fabry disease, is a rare genetic disease that can affect many parts of the body, including the kidneys, heart, and skin. Fabry disease is one of a group of conditions known as lysosomal storage diseases. The genetic mutation that causes Fabry disease interferes with the function of an enzyme that processes biomolecules known as sphingolipids, leading to these substances building up in the walls of blood vessels and other organs. It is inherited in an X-linked manner.
has abstract
Anderson-Fabrys sjukdom tillhö ...... olika personer med sjukdomen.
@sv
Choroba Fabry'ego (choroba And ...... ie w sposób sprzężony z płcią.
@pl
De ziekte van Fabry of angioke ...... rouwen ook symptomatisch zijn.
@nl
Doença de Fabry, doença de And ...... total ausência ou deficiência.
@pt
Fabry disease, also known as A ...... geon William Anderson in 1898.
@en
La enfermedad de Fabry es una ...... por almacenamiento de lípidos.
@es
La maladie de Fabry, ou syndro ...... sylceramide dans les cellules.
@fr
La malaltia de Fabry, també co ...... matòleg i el cirurgià el 1898.
@ca
La malattia di Fabry è un'anom ...... attie da accumulo lisosomiale.
@it
Боле́знь Фабри́ (болезнь Андер ...... пектром клинических симптомов.
@ru
complications
Heart failure,abnormal heart rhythms
differential diagnosis
DiseasesDB
eMedicine subject
neuro
@en
eMedicine topic
579
@en
geneReviewsId
geneReviewsName
Fabry disease
@en
ICD10
medical diagnosis
MeSH ID
OMIM id
Link from a Wikipage to an external page
Wikipage page ID
page length (characters) of wiki page
Wikipage revision ID
1,025,963,134
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caption
Alpha galactosidase - the deficient protein in Fabry disease
@en
causes
Genetic
@en
complications
diagnosis
Enzyme activity assay, genetic testing
@en
differential
DiseasesDB
eMedicineSubj
neuro
@en
eMedicineTopic
GeneReviewsName
Fabry disease
@en
GeneReviewsNBK
NBK1292
@en
ICD
MeshID
D000795
@en
name
Fabry disease
@en
OMIM
onset
Childhood
@en
specialty
Endocrinology, cardiology, nephrology, dermatology
@en
synonyms
Fabry's disease, Anderson–Fabr ...... pha-galactosidase A deficiency
@en
treatment
Enzyme replacement
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wikiPageUsesTemplate
wordnet_type
subject
hypernym
comment
Anderson-Fabrys sjukdom tillhö ...... olika personer med sjukdomen.
@sv
Choroba Fabry'ego (choroba And ...... wnie w sposób sprzężony z płci
@pl
De ziekte van Fabry of angioke ...... n het enzym α-galactosidase A.
@nl
Doença de Fabry, doença de And ...... total ausência ou deficiência.
@pt
Fabry disease, also known as A ...... herited in an X-linked manner.
@en
La enfermedad de Fabry es una ...... por almacenamiento de lípidos.
@es
La maladie de Fabry, ou syndro ...... sylceramide dans les cellules.
@fr
La malaltia de Fabry, també co ...... sos sanguinis i altres òrgans.
@ca
La malattia di Fabry è un'anom ...... attie da accumulo lisosomiale.
@it
Боле́знь Фабри́ (болезнь Андер ...... пектром клинических симптомов.
@ru
label
Anderson-Fabrys sjukdom
@sv
Choroba Fabry’ego
@pl
Doença de Fabry
@pt
Enfermedad de Fabry
@es
Fabry disease
@en
Maladie de Fabry
@fr
Malaltia de Fabry
@ca
Malattia di Fabry
@it
Morbus Fabry
@de
Ziekte van Fabry
@nl
sameAs
closeMatch
wasDerivedFrom
isPrimaryTopicOf
name
Fabry disease
@en