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Genetic disorders
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From Canonica AI
Pages in category "Genetic disorders"
The following 82 pages are in this category, out of 82 total.
3
3-hydroxyacyl-CoA dehydrogenase
A
Acatalasia
Adenosine Deaminase Deficiency
Adrenoleukodystrophy
Advanced sleep phase disorder
Albright hereditary osteodystrophy
Aniridia
Arginase
Argininosuccinate lyase
Aromatic L-amino acid decarboxylase
Autosomal Recessive Disorders
B
Bardet-Biedl Syndrome
Becker muscular dystrophy
Bloom syndrome
C
Carbamoyl phosphate synthetase
Carbamoyl Phosphate Synthetase II
Catecholaminergic polymorphic ventricular tachycardia
Chromosomal disorders
Chromosome 13
Ciliopathies
Common Variable Immunodeficiency
Complex disorder
CREBBP
Cystic fibrosis
D
Disorders of sexual differentiation
Dwarfism in Biology
Dyskeratosis congenita
F
Facioscapulohumeral muscular dystrophy
Familial chylomicronemia syndrome
Fanconi anemia
Fragile X Syndrome
G
Galactose
Gaucher's disease
Genetic Disease
H
Hemochromatosis
Hereditary spastic paraplegia
Huntington's disease
Hyper IgE Syndrome
Hyperlipidemia
Hypertrophic cardiomyopathy
I
Ichthyosis
L
Leber's hereditary optic neuropathy
Leloir pathway
Lesch-Nyhan Syndrome
Leucism
Limb-girdle muscular dystrophy
Long QT syndrome
Lymphangioleiomyomatosis
M
MELAS
Metabolic Disorders
Methemoglobinemia
Microorchidism
Mitochondrial myopathy
Mucopolysaccharidosis
Multiple endocrine neoplasia type 1
Muscle disease
Muscular Dystrophy
N
N-acetylglutamate
Neurofibromatosis type 1
Neuromuscular disease
Niemann-Pick Disease
Noonan Syndrome
O
Osteogenesis imperfecta
P
Polycythemia
Polydactyly
Primary Ciliary Dyskinesia
PRPP synthetase
Pseudohypoparathyroidism
R
Retinitis pigmentosa
Ribosomopathies
S
S-adenosylhomocysteine hydrolase
Single-gene disorders
Spinal Muscular Atrophy
Synpolydactyly
T
Tay-Sachs Disease
Thalassemia
Turner Syndrome
V
Von Willebrand Disease
W
WAGR syndrome
Werner Syndrome
Wiskott-Aldrich Syndrome
X
Xxy
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