Fabry disease
0 sources
Fabry disease
Summary
Fabry disease is a developmental defect during embryogenesis[1]. It ranks in the top 6% of developmental_defect_during_embryogenesis entities by monthly Wikipedia readership (328 views/month).[2]
Key Facts
- Fabry disease's image is recorded as PBB Protein GLA image.jpg[3].
- Fabry disease's instance of is recorded as developmental defect during embryogenesis[4].
- Fabry disease's instance of is recorded as rare disease[5].
- Fabry disease's instance of is recorded as genetic disease[6].
- Fabry disease's instance of is recorded as class of disease[7].
- Fabry disease's instance of is recorded as symptom or sign[8].
- Johannes Fabry is named after Fabry disease[9].
- Fabry disease's GND ID is recorded as 4153455-4[10].
- Fabry disease's subclass of is recorded as sphingolipidosis[11].
- Fabry disease's subclass of is recorded as developmental anomaly of metabolic origin[12].
- Fabry disease's subclass of is recorded as genetic skin vascular disorder[13].
- Fabry disease's subclass of is recorded as rare genetic epilepsy[14].
- Fabry disease's subclass of is recorded as syndromic dyslipidemia[15].
- Fabry disease's subclass of is recorded as vascular skin disease[16].
- Fabry disease's subclass of is recorded as hypertrophic cardiomyopathy[17].
- Fabry disease's subclass of is recorded as sphingolipidosis with epilepsy[18].
- Fabry disease's subclass of is recorded as syndromic lymphedema[19].
- Fabry disease's subclass of is recorded as nephropathy secondary to a storage or other metabolic disease[20].
- Fabry disease's subclass of is recorded as cataract associated with a metabolic disease[21].
- Fabry disease's subclass of is recorded as metabolic disease with corneal opacity[22].
- Fabry disease's subclass of is recorded as lysosomal disease with restrictive cardiomyopathy[23].
- Fabry disease's subclass of is recorded as lysosomal disease with hypertrophic cardiomyopathy[24].
- Fabry disease's subclass of is recorded as rare hereditary metabolic disease with peripheral neuropathy[25].
- Fabry disease's subclass of is recorded as syndrome associated with hypertrophic cardiomyopathy[26].
- Fabry disease's subclass of is recorded as disease[27].
Why It Matters
Fabry disease ranks in the top 6% of developmental_defect_during_embryogenesis entities by monthly Wikipedia readership (328 views/month).[2] It has Wikipedia articles in 18 language editions, a strong signal of global cultural recognition.[28] It is known by 26 alternative names across languages and contexts.[29]