Condition specific information

This page contains links to Covid-19 condition specific information. If you would like to submit condition specific Covid-19 information for inclusion please email covid-19@geneticalliance.org.uk. If you are looking for information about Covid-19 guidance please check out the country specific pages for England, Wales, Scotland and Northern Ireland. Please note - these links will take you to external web pages and Genetic Alliance UK takes no responsibility for their content.

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22q11.2 deletion syndrome

Information about Covid-19 and 22q11.2 deletion syndrome

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Alkaptonuria (AKU)

Information about Covid-19 and AKU

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Alpha-1 Antitrypsin Deficiency

Information about Covid-19 and alpha-1 antitrypsin deficiency

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Alpha-1 Antitrypsin Deficiency.

Information about Covid-19 and alpha-1 antitrypsin deficiency.

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Alstrom Syndrome

Information about Covid-19 and Alstrom Syndrome

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Angelman Syndrome

Information about Covid-19 and Angelman Syndrome

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Ataxia

Information about Covid-19 and ataxia

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Ataxia-Telangiectasia

Information about Covid-19 and Ataxia-Telangiectasia

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Barth Syndrome

Information about Covid-19 and Barth Syndrome

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Beckwith-Wiedeman Syndrome (BWS)

Information about Covid-19 and BWS

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Behçet’s Syndrome

Information about Covid-19 and Behçet's Syndrome

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Cardiomyopathy

Information about Covid-19 and cardiomyopathy

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Cavernoma

Information about Covid-19 and Cavernoma

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Charcot-Marie-Tooth Disease

Information about covid-19 and CMT

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Childhood Cancer and Leukaemia

Information about covid-19 and Childhood Cancer and Leukaemia

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Childhood Deafness

Information about Covid-19 and Childhood Deafness

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Childhood Liver Disease

Information about covid-19 and Childhood Liver Disease

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Chronic Granulomatous Disease

Information about Covid-19 and CGD

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Cockayne Syndrome (CS) and Trichothiodystrophy (TTD)

Information about Covid-19 and Cockayne Syndrome (CS) and Trichothiodystrophy (TTD)

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Congenital disorders of glycosylation (CDG)

Information about Covid-19 and CDG

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Cornelia de Lange Syndrome (CdLS)

Information about Covid-19 and CdLS

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Cystic Fibrosis (CF)

Information about Covid-19 and cystic fibrosis

The impact of coronavirus on your CF care

Coronavirus and face masks

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Dementia

Information about Covid-19 and Dementia

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Dravet Syndrome

Information about Covid-19 and Dravet Syndrome

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Duchenne Muscular Dystrophy

Information about Covid-19 and DMD

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Ectodermal Dysplasia (EDS)

Information about Covid-19 and EDS

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Ehlers-Danlos Syndrome (EDS)

Information about Covid-19 and EDS

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Ehlers-Danlos Syndrome (EDS), hypermobility spectrum disorders (HSD), and related conditions

Information about Covid-19 and EDS

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Endocrine Conditions

Information about Covid-19 and endocrine conditions

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Eye Conditions

Information about Covid-19 and eye conditions

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Fanconi Anaemia

Information about Covid-19 and fanconi anaemia

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Fibrous Dysplasia

Information about covid-19 and fibrous dysplasia

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Gaucher Disease

Information about Covid-19 and Gaucher Disease

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Genetic Disorders

Information about Covid-19 and genetic disorders

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Glycogen Storage Disease

Information about Covid-19 and glycogen storage disease

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Growth and Endocrine Issues

Information about covid-19 and Growth and Endocrine Issues

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Haemochromatosis

Information about Covid-19 and Haemochromatosis

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Haemophilia

Information about Covid-19 and Haemophilia

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Heart or circulatory disease

Information about Covid-19 and heart or circulatory disease

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Hereditary Angioedema (HAE)

Information about Covid-19 and HAE

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Hereditary Spastic Paraplegia (HSP)

Information about Covid-19 and Hereditary Spastic Paraplegia (HSP)

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Huntington’s Disease

Information about Covid-19 and Huntington's Disease

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Hyperinsulinism

Information about Covid-19 and Hyperinsulinism

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Ichthyosis

Information about Covid-19 and Ichthyosis

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Idiopathic Intracranial Hypertension

Information about Covid-19 and IIH

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Inherited metabolic disorders

Information about Covid-19 and inherited metabolic disorders

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Klinefelter’s Syndrome

Information about Covid-19 and Klinefelter's Syndrome

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Leukodystrophy

Information on Covid-19 and leukodystrophy

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Mitochondrial Disorders

Information about Covid-19 and mitochondrial disorders

Emerging from lockdown – guidance for shielding patients and families

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Motor Neurone Disease

Information about Covid-19 and MND

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MPS (Mucopolysaccharide), Fabry and related disorders.

Information about Covid-19 and MPS (Mucopolysaccharide), Fabry and related disorders.

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Multiple system atrophy (MSA)

Information about Covid-19 and MSA

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Muscular Dystrophy and Muscle Wasting Conditions

Information about Covid-19 and Muscular Dystrophy

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Neurofibromatosis

Information about Covid-19 and neurofibromatosis

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Neurofibromatosis (NF)

Information about Covid-19 and Neurofibromatosis (NF)

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Neurological Conditions

Information on Covid-19 and neurological conditions from the British Paediatric Neurology Asssociation

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Neurological Conditions

Information about Covid-19 and neurological conditions

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Niemann-Pick Disease

Information about Covid-19 and Niemann-Pick Disease

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Osteogenesis Imperfecta

Information on Covid-19 and Osteogenesis Imperfecta

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Pituitary Conditions

Information about Covid-19 and Pituitary Conditions

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Polycystic Kidney Disease

Information about Covid-19 and polycystic kidney disease

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Porphyria

Information about Covid-19 and Porphyria

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Primary Ciliary Dyskinesia

Information about Covid-19 and Primary Ciliary Dyskinesia

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Primary Immune Deficiencies

Information about Covid-19 and primary immune deficiency

COVID-19 and your emotional wellbeing

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Primary Sclerosing Cholangitis (PSC)

Information about Covid-19 and primary sclerosing cholangitis (PSC)

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Pulmonary Hypertension (PH)

Information about Covid-19 and Pulmonary Hypertension (PH)

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Rare Chromosome and Gene Disorders

Information about Covid-19 and Rare Chromosome and Gene Disorders

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Rare Kidney Diseases

Information about Covid-19 and rare kidney diseases

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Rett syndrome

Information about Covid-19 and Rett Syndrome

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Rett Syndrome

Information about Covid-19 and Rett syndrome

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Ring 20 syndrome

Information about Covid-19 and Ring 20 syndrome

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Scleroderma and Raynaud’s disease

Information about Covid-19 and Scleroderma and Raynaud's disease

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Shwachman-Diamond Syndrome

Information about Covid-19 and Shwachman-Diamond Syndrome

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Sickle Cell Disorder

Information about Covid-19 and Sickle Cell Disorder

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Spinal Muscular Atrophy (SMA)

Information about Covid-19 and spinal muscular atrophy (SMA)

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Spinal Muscular Atrophy (SMA)

Information about Covid-19 and SMA

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Spontaneous Coronary Artery Dissection (SCAD)

Information about Covid-19 and SCAD

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Thalassaemia

Statement about Covid-19 and Thalassaemia

Information about Covid-19 and Thalassaemia

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Thrombotic Thrombocytopenic Purpura (TTP)

Information about Covid-19 and TTP

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Thyroid conditions

Information about Covid-19 and thyroid conditions

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Tourette Syndrome

Information about Covid-19 and Tourette Syndrome

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Tracheo-Oesophageal Fistula Conditions

Information about Covid-19 and TOF conditions

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Tuberous Sclerosis

Information about Covid-19 and Tuberous Sclerosis

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Turner Syndrome

Information about Covid-19 and Turner syndrome

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Undiagnosed genetic conditions

Information about Covid-19 and undiagnosed genetic conditions

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Vascular Ehlers Danlos Syndrome (EDS)

Information on Covid-19 and Vascular EDS

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Vasculitis

Information about Covid-19 and Vasculitis

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Williams Syndrome

Information on Covid-19 and Williams Syndrome

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Wolfram Syndrome

Information about Covid-19 and wolfram syndrome

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The economic and social implications of the coronavirus crisis are already having profound impacts on individuals and families affected by genetic, rare and undiagnosed conditions, as well as on the voluntary organisations and charities that support them. The impact of Covid-19 on the charity sector is devastating. Many charities are struggling to support their communities and wondering if they will survive. We are working hard to support all our members and the wider genetic, rare and undiagnosed community but we share their concerns - please help us help them.

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