Results 81 -
88
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88
for
Autosomal dominant inheritance
- Acute Intermittent Porphyria (AIP) (American Porphyria Foundation)Porphyria/Specifics ... Porphyria ... American Porphyria Foundation
- 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) ...
- Guide to Understanding Pfeiffer Syndrome (Children's Craniofacial Association) - PDFCraniofacial Abnormalities/Specifics ... Craniofacial Abnormalities ... Children's Craniofacial Association ... PDF
- Alport Syndrome (National Kidney Foundation)Hearing Disorders and Deafness/Specifics ... Hearing Disorders and Deafness ... Kidney Diseases/Specifics ... Kidney Diseases ... National Kidney Foundation ... Alport syndrome ...
- Leukodystrophies/Specifics ... Leukodystrophies ... National Institute of Neurological Disorders and Stroke ... From the National Institutes of Health ... Aicardi-Goutières ...
- Dementia/Start Here ... Dementia ... Lewy Body Dementia/Statistics and Research ... Lewy Body Dementia ... National Institute of Neurological Disorders and Stroke ... From the ...
- Rare Clotting Factor Deficiencies (World Federation of Hemophilia)Bleeding Disorders/Specifics ... Bleeding Disorders ... Vitamin K/Learn More ... Vitamin K ... World Federation of Hemophilia
- Immune System and Disorders/Specifics ... Immune System and Disorders ... DOCK8 deficiency is a rare immune disorder named after the mutated gene which NIAID scientists ...