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Mucolipidoses
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3-Hydroxyacyl-Coa Dehydrogenase Deficiency
Al-Raqad Syndrome
Arthrochalasia Ehlers-Danlos Syndrome
Blood Group, Dombrock System
Blood Group, I System
Carpal Tunnel Syndrome
Doyne Honeycomb Retinal Dystrophy
Fanconi Anemia, Complementation Group E
Glycoproteinosis
Hydrops Fetalis
Hydrops Fetalis, Nonimmune, and/or Atrial Septal Defect
Learning Disability
Linear Skin Defects with Multiple Congenital Anomalies 1
Lysosomal Storage Disease
Mcleod Syndrome
Mononeuropathy of the Median Nerve, Mild
Mucolipidosis Iii Alpha/beta
Mucolipidosis Iv
Mucopolysaccharidoses
Mucopolysaccharidosis-Plus Syndrome
Myoclonus
Neuraminidase Deficiency
Spastic Ataxia, Charlevoix-Saguenay Type
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