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Results 81 - 88 of 88 for Autosomal dominant inheritance
  1. Acute Intermittent Porphyria (AIP) (American Porphyria Foundation)  
    Porphyria/Specifics ... Porphyria ... American Porphyria Foundation
  2. Osteochondroma (American Academy of Orthopaedic Surgeons)  
    Benign Tumors/Specifics ... Benign Tumors ... Bone Diseases/Specifics ... Bone Diseases ... American Academy of Orthopaedic Surgeons ... An osteochondroma is a benign (noncancerous) ...
  3. Guide to Understanding Pfeiffer Syndrome (Children's Craniofacial Association) - PDF  
    Craniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... Children's Craniofacial Association ... PDF
  4. Alport Syndrome (National Kidney Foundation)  
    Hearing Disorders and Deafness/Specifics ... Hearing Disorders and Deafness ... Kidney Diseases/Specifics ... Kidney Diseases ... National Kidney Foundation ... Alport syndrome ...
  5. Aicardi-Goutieres Syndrome From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Leukodystrophies/Specifics ... Leukodystrophies ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Aicardi-Goutières ...
  6. Dementias From the National Institutes of Health (National Institute of Neurological Disorders and Stroke)  
    Dementia/Start Here ... Dementia ... Lewy Body Dementia/Statistics and Research ... Lewy Body Dementia ... National Institute of Neurological Disorders and Stroke ... From the ...
  7. Rare Clotting Factor Deficiencies (World Federation of Hemophilia)  
    Bleeding Disorders/Specifics ... Bleeding Disorders ... Vitamin K/Learn More ... Vitamin K ... World Federation of Hemophilia
  8. DOCK8 Deficiency From the National Institutes of Health (National Institute of Allergy and Infectious Diseases)  
    Immune System and Disorders/Specifics ... Immune System and Disorders ... DOCK8 deficiency is a rare immune disorder named after the mutated gene which NIAID scientists ...
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