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How Long To Get My DNA Test Results?
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How Do DNA Tests Work?
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Genetic Counseling
The Ultimate Guide to Genetic Counselors
What Genetic Counselors Do: Explained
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Ultimate Guide to DNA Test Results
What Is GEDMatch? How Does It Work?
Guide to NIPT Tests and Prenatal Testing
CAR T-Cell Therapy
Ultimate Guide to Carrier Screening
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Science & Disease
Rare Diseases
Ichthyosis: Rare Genetic Skin Disorder
Huntington's Disease
CREST Syndrome Genetic Disorder
Stevens-Johnson Syndrome Genetic Disorder
Prader Willi Syndrome
Cat Eye Syndrome
Angelman Syndrome: Genetic Disorder
Stromme Syndrome
The Ultimate Guide to Klotho
How Many Rare Diseases Are There?
Duchenne Muscular Dystrophy: Genetic Disorder
The PKU (Phenylketonuria) Test
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Science
What is a Haplotype? What is a Haplogroup?
What is Mitochondrial DNA?
How Long is a Generation?
Autosomal DNA (Definition)
MTHFR Gene Mutations and DNA Tests
APOE
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Health
DNA Tests for Leukemia
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Best Genetic (DNA) Tests For Cancer Risk
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Best DNA Tests for Ancestry
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What Is CRISPR?
Luna DNA
Nebula Genomics
What Is Color Genomics?
TeloYears Genetic Test
Klotho
SneakPeek Early Gender DNA Test
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YourDNA
Rare Diseases
Rare Diseases
Start Here
Angelman Syndrome: Genetic Disorder Diagnosis and More
CREST Syndrome Genetic Disorder (Guide)
Cat Eye Syndrome
Duchenne Muscular Dystrophy: Genetic Disorder {Guide}
How Many Rare Diseases Are There?
Huntington's Disease Genetic Disorder: Treatment Options & Diagnosis
Ichthyosis: Rare Genetic Skin Disorder
Prader Willi Syndrome
Stevens-Johnson Syndrome Genetic Disorder (Guide)
Stromme Syndrome: Symptoms, Treatment Options and Your Plan of Action
The PKU (Phenylketonuria) Test
The Ultimate Guide to Klotho
All in Rare Diseases
A Guide to Down Syndrome
ALD Symptoms and Diagnosis
Alport Syndrome
Amniotic Band Syndrome
An Overview of Shy Drager Syndrome (Multiple System Atrophy)
Batten Disease Symptoms & Diagnosis
Canavan Disease
Charge Syndrome
Congenital Adrenal Hyperplasia
Cornelia de Lange Syndrome
Cystic Fibrosis
Dahm Triplets DNA Test
Dermatomyositis
Dravet Syndrome: A Genetic Disorder Guide
Dystonia Genetic Disorder (Guide)
Fabry Disease
Familial Mediterranean Fever (FMF)
Fragile X Syndrome
Galactosemia Disease
Gaucher Disease
Genetic Tests for Autism
Gliomatosis Cerebri
Guide to Megaesophagus
Hemochromatosis
Hemophilia A
How likely am I to inherit a rare disease?
Klinefelter Syndrome
Korsakoff Syndrome
Limb-Girdle Muscular Dystrophy (LGMD)
Maple Syrup Urine Disease
McArdle Disease
Misophonia
Myotonic Dystrophy
Neurofibromatosis (NF) Symptoms, Treatment and More
Neurofibromatosis Type 1
Nonketotic Hyperglycinemia
Oculocutaneous Albinism
Phenylketonuria: Genetic Disorder
Polycystic Kidney Disease
Pompe Disease
Prune Belly Syndrome Symptoms & Diagnosis
Prurigo
Renal Tubular Acidosis
Rett Syndrome
Sickle Cell Anemia
Tay-Sachs Genetic Disorder {Guide}
Ultimate Guide to Diabetes
Ultimate Guide to Inherited Cancer & Genomics
Ultimate Guide to Rare Diseases
VHL (Von Hippel-Lindau Tumor Suppressor)
VLCAD — VLCADD
What Is Achalasia? (A Guide)
What Is Brugada Syndrome?
What Is Cholelithiasis?
What Is Dermatitis Herpetiformis? (A Guide)
What Is Leber Congenital Amaurosis?
What You Should Know About Keratoconus
What to Know About Bloom Syndrome (BSyn)
What to Know About G6PD Deficiency
What to Know About Thalassemia
Which Rare Diseases Are the Most Common?
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More Reading
How Long to Get My DNA Test Results?
How Much Do DNA Tests Cost?
The MTHFR Gene Mutation
CAR T-Cell Therapy Guide
Rare Disease: Huntington's Disease
What is Fabry Disease?
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Cure Rare Disease
Read more about our partner Cure Rare Disease and the fight against Duchenne’s.
The Number of Rare Diseases?
How many rare diseases are there? Read our guide here.
Ultimate Guide to Genetic Counselors
Genetic counselors play a vital role in the process of understanding your test results.
Speak with a Genetic Counselor
Genetic counselors are certified professionals who help patients understand the results of genetic testing. Curious about your test results? Need to speak with someone directly?
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