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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.

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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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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.

22q11.2 deletion syndrome

Alkaptonuria (AKU)

Alpha-1 Antitrypsin Deficiency

Alpha-1 Antitrypsin Deficiency.

Alstrom Syndrome

Angelman Syndrome

Ataxia

Ataxia-Telangiectasia

Barth Syndrome

Beckwith-Wiedeman Syndrome (BWS)

Behçet’s Syndrome

Cardiomyopathy

Cavernoma

Charcot-Marie-Tooth Disease

Childhood Cancer and Leukaemia

Childhood Deafness

Childhood Liver Disease

Chronic Granulomatous Disease

Cockayne Syndrome (CS) and Trichothiodystrophy (TTD)

Congenital disorders of glycosylation (CDG)

Cornelia de Lange Syndrome (CdLS)

Cystic Fibrosis (CF)

Dementia

Dravet Syndrome

Duchenne Muscular Dystrophy

Ectodermal Dysplasia (EDS)

Ehlers-Danlos Syndrome (EDS)

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

Endocrine Conditions

Eye Conditions

Fanconi Anaemia

Fibrous Dysplasia

Gaucher Disease

Genetic Disorders

Glycogen Storage Disease

Growth and Endocrine Issues

Haemochromatosis

Haemophilia

Heart or circulatory disease

Hereditary Angioedema (HAE)

Hereditary Spastic Paraplegia (HSP)

Huntington’s Disease

Hyperinsulinism

Ichthyosis

Idiopathic Intracranial Hypertension

Inherited metabolic disorders

Klinefelter’s Syndrome

Leukodystrophy

Mitochondrial Disorders

Motor Neurone Disease

MPS (Mucopolysaccharide), Fabry and related disorders.

Multiple system atrophy (MSA)

Muscular Dystrophy and Muscle Wasting Conditions

Neurofibromatosis

Neurofibromatosis (NF)

Neurological Conditions

Neurological Conditions

Niemann-Pick Disease

Osteogenesis Imperfecta

Pituitary Conditions

Polycystic Kidney Disease

Porphyria

Primary Ciliary Dyskinesia

Primary Immune Deficiencies

Primary Sclerosing Cholangitis (PSC)

Pulmonary Hypertension (PH)

Rare Chromosome and Gene Disorders

Rare Kidney Diseases

Rett syndrome

Rett Syndrome

Ring 20 syndrome

Scleroderma and Raynaud’s disease

Shwachman-Diamond Syndrome

Sickle Cell Disorder

Spinal Muscular Atrophy (SMA)

Spinal Muscular Atrophy (SMA)

Spontaneous Coronary Artery Dissection (SCAD)

Thalassaemia

Thrombotic Thrombocytopenic Purpura (TTP)

Thyroid conditions

Tourette Syndrome

Tracheo-Oesophageal Fistula Conditions

Tuberous Sclerosis

Turner Syndrome

Undiagnosed genetic conditions

Vascular Ehlers Danlos Syndrome (EDS)

Vasculitis

Williams Syndrome

Wolfram Syndrome