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Genetic disorders
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From Canonica AI
Pages in category "Genetic disorders"
The following 66 pages are in this category, out of 66 total.
3
3-hydroxyacyl-CoA dehydrogenase
A
Acatalasia
Adenosine Deaminase Deficiency
Adrenoleukodystrophy
Advanced sleep phase disorder
Aniridia
Arginase
Argininosuccinate lyase
Autosomal Recessive Disorders
B
Bardet-Biedl Syndrome
Bloom syndrome
C
Carbamoyl phosphate synthetase
Carbamoyl Phosphate Synthetase II
Catecholaminergic polymorphic ventricular tachycardia
Chromosome 13
Ciliopathies
Common Variable Immunodeficiency
Complex disorder
CREBBP
Cystic fibrosis
D
Dwarfism in Biology
Dyskeratosis congenita
F
Familial chylomicronemia syndrome
Fanconi anemia
Fragile X Syndrome
G
Galactose
H
Hemochromatosis
Hereditary spastic paraplegia
Huntington's disease
Hyperlipidemia
Hypertrophic cardiomyopathy
I
Ichthyosis
L
Leber's hereditary optic neuropathy
Leloir pathway
Lesch-Nyhan Syndrome
Leucism
Long QT syndrome
Lymphangioleiomyomatosis
M
Metabolic Disorders
Microorchidism
Mitochondrial myopathy
Mucopolysaccharidosis
Multiple endocrine neoplasia type 1
Muscle disease
Muscular Dystrophy
N
N-acetylglutamate
Neurofibromatosis type 1
Neuromuscular disease
Noonan Syndrome
O
Osteogenesis imperfecta
P
Polycythemia
Polydactyly
Primary Ciliary Dyskinesia
Pseudohypoparathyroidism
R
Retinitis pigmentosa
Ribosomopathies
S
S-adenosylhomocysteine hydrolase
Spinal Muscular Atrophy
Synpolydactyly
T
Tay-Sachs Disease
Thalassemia
Turner Syndrome
V
Von Willebrand Disease
W
Werner Syndrome
Wiskott-Aldrich Syndrome
X
Xxy
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