Results 71 -
80
of
88
for
Autosomal dominant inheritance
- Mineral and Bone Disorder in Chronic Kidney Disease
(National Institute of Diabetes and Digestive and Kidney Diseases)
Kidney Failure/Related Issues ... Kidney Failure ... Chronic Kidney Disease/Related Issues ... Chronic Kidney Disease ... Dialysis/Related Issues ... Dialysis ... Parathyroid Disorders/ ... - Resources about some of the forms of primary immune deficiency diseases (PIDDs) which NIAID is currently studying. ... Immune System and Disorders/Specifics ...
- Causes of Cardiomyopathy (Children's Cardiomyopathy Foundation)Cardiomyopathy/Children ... Cardiomyopathy ... Children's Cardiomyopathy Foundation
- Marfan Syndrome (For Parents) (Nemours Foundation)... dissections, aorta, myopia, nearsightedness, detached retinas, glaucoma, cataracts, autosomal dominant, arms and legs, long arms and legs, connective ...
- Multiple Endocrine Neoplasia Type I
(National Institute of Diabetes and Digestive and Kidney Diseases)
Pheochromocytoma/Related Issues ... Pheochromocytoma ... Endocrine Diseases/Specifics ... Endocrine Diseases ... Parathyroid Disorders/Specifics ... Parathyroid Disorders ... Benign ... - Noonan Syndrome (For Parents) (Nemours Foundation)... syndrome, Hypertelorism, Cardiofaciocutaneous syndrome, Short stature, growth hormone, autosomal dominant, Lordosis, Pulmonary valvular stenosis, typical face dysmorphology, congenital ...
- Friedreich's Ataxia (FA) (Muscular Dystrophy Association)Friedreich Ataxia/Start Here ... Friedreich Ataxia ... Muscular Dystrophy Association ... MDA is the #1 health nonprofit advancing research, care and advocacy for people ...
- Genetic Disorders/Start Here ... Genetic Disorders ... National Human Genome Research Institute ... From the National Institutes of Health ... A list of genetic, orphan and ...
- Ataxias and Cerebellar or Spinocerebellar Degeneration
(National Institute of Neurological Disorders and Stroke)
Friedreich Ataxia/Related Issues ... Friedreich Ataxia ... Cerebellar Disorders/Start Here ... Cerebellar Disorders ... National Institute of Neurological Disorders and Stroke - 22q11.2 Deletion Syndrome (DiGeorge Syndrome) (For Parents) (Nemours Foundation)... 22q, 22q11.2DS, DiGeorge syndrome, DiGeorge, Shprintzen Syndrome, autosomal dominant OpitzG, Cayler Cardiofacial Syndrome, cardiofacial, Conotruncal Anomaly Face ...