Category:Unknown-importance medical genetics articles
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Pages in category "Unknown-importance medical genetics articles"
The following 200 pages are in this category, out of approximately 699 total. This list may not reflect recent changes.
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- Talk:G protein-coupled receptor kinase 3
- Talk:Galactosialidosis
- Talk:Ayelet Galena
- Talk:Galloway–Mowat syndrome
- Talk:GAPO syndrome
- Talk:Gardner's syndrome
- Talk:Gaucher's disease
- Talk:Gene duplication
- Talk:Gene therapy for color blindness
- Talk:Gene therapy for epilepsy
- Talk:Gene therapy for osteoarthritis
- Talk:Gene therapy in Parkinson's disease
- Talk:Gene Wiki
- Talk:GeneMatcher
- Talk:Genetic disorder
- Talk:Genetic epidemiology
- Talk:Genetic heterogeneity
- Talk:Genetic marker
- Talk:Genetic screen
- Talk:Genetic testing
- Talk:Genetics
- Talk:Genetics of aging
- Talk:Genetics of Down syndrome
- Talk:Genetics of infertility
- Talk:Genitopatellar syndrome
- Talk:Genomics
- Talk:Deborah German
- Talk:Germline mosaicism
- Talk:Germline mutation
- Talk:Giant axonal neuropathy
- Talk:Gilbert's syndrome
- Talk:Glanzmann's thrombasthenia
- Talk:Glutaric acidemia type 2
- Talk:Glutaric aciduria type 1
- Talk:Gluten immunochemistry
- Talk:Glycogen storage disease type I
- Talk:Glycogen storage disease type II
- Talk:Glycogen storage disease type III
- Talk:GM2 gangliosidoses
- Talk:GRACILE syndrome
- Talk:Greig cephalopolysyndactyly syndrome
- Talk:Gulf War syndrome
- Talk:Gustavson syndrome
- Talk:Robert Guthrie (microbiologist)
H
- Talk:Haemophilia
- Talk:Haemophilia A
- Talk:Haemophilia B
- Talk:Haemophilia C
- Talk:Haemophilia in European royalty
- Talk:Hajdu–Cheney syndrome
- Talk:Hallermann–Streiff syndrome
- Talk:Harlequin-type ichthyosis
- Talk:Hawkinsinuria
- Talk:Hemiplegic migraine
- Talk:Hemoglobin Hopkins-2
- Talk:Hereditary elliptocytosis
- Talk:Hereditary fructose intolerance
- Talk:Hereditary hemorrhagic telangiectasia
- Talk:Hereditary motor and sensory neuropathy
- Talk:Hereditary multiple exostoses
- Talk:Hereditary nonpolyposis colorectal cancer
- Talk:Hereditary spastic paraplegia
- Talk:Heredity in Relation to Eugenics
- Talk:Heritability of autism
- Talk:Heteroplasmy
- Talk:History of Asperger syndrome
- Talk:HLA-DQ1
- Talk:HLA-DQB1
- Talk:Andrew Holding
- Talk:John Holloway (geneticist)
- Talk:Holocarboxylase synthetase deficiency
- Talk:Holt–Oram syndrome
- Talk:Homocystinuria
- Talk:Human behaviour genetics
- Talk:Hunter syndrome
- Talk:Huntingtin-interacting protein 1
- Talk:Huntington's disease-like syndrome
- Talk:Hurler syndrome
- Talk:Hyperglycerolemia
- Talk:Hyperkalemic periodic paralysis
- Talk:Hypochondrogenesis
- Talk:Hypochondroplasia
- Talk:Hypohidrotic ectodermal dysplasia
- Talk:Hypokalemic periodic paralysis
- Talk:Hypomagnesemia with secondary hypocalcemia
I
- Talk:Ichthyosis vulgaris
- Talk:Immunodeficiency–centromeric instability–facial anomalies syndrome
- Talk:Inborn errors of immunity
- Talk:Inbreeding
- Talk:Incontinentia pigmenti
- Talk:Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
- Talk:Infantile cortical hyperostosis
- Talk:Intellectual disability-spasticity-ectrodactyly syndrome
- Talk:Interferon-induced transmembrane protein 5
- Talk:Internexin
- Talk:Intraepithelial lymphocyte
- Talk:Iris hypoplasia with glaucoma
- Talk:Isobutyryl-coenzyme A dehydrogenase deficiency
- Talk:Isodicentric 15
- Talk:Isogenic human disease models
- Talk:Isolated growth hormone deficiency
- Talk:Isovaleric acidemia
J
K
- Talk:Kabuki syndrome
- Talk:Emil Kakkis
- Talk:Kallmann syndrome
- Talk:Karyotype
- Talk:Katz syndrome
- Talk:KBG syndrome
- Talk:KCNQ2 developmental and epileptic encephalopathy
- Talk:Kearns–Sayre syndrome
- Talk:Kindler syndrome
- Talk:Klinefelter syndrome
- Talk:Klippel–Feil syndrome
- Talk:Kniest dysplasia
- Talk:Koolen–De Vries syndrome
- Talk:Krabbe disease
L
- Talk:Lactose intolerance
- Talk:Langer–Giedion syndrome
- Talk:Laron syndrome
- Talk:Larsen syndrome
- Talk:Late onset congenital adrenal hyperplasia
- Talk:Laurence–Moon syndrome
- Talk:Leber's hereditary optic neuropathy
- Talk:Leigh syndrome
- Talk:Lethal white syndrome
- Talk:Leukocyte adhesion deficiency
- Talk:Leukocyte adhesion deficiency-1
- Talk:Leukoencephalopathy with vanishing white matter
- Talk:Li–Fraumeni syndrome
- Talk:Lipid storage disorder
- Talk:Lipoid congenital adrenal hyperplasia
- Talk:List of disorders included in newborn screening programs
- Talk:List of people with color blindness
- Talk:Loading control
- Talk:Loeys–Dietz syndrome
- Talk:Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
- Talk:Long-term nonprogressor
- Talk:Lysinuric protein intolerance
M
- Talk:Madelung's deformity
- Talk:Mahvash disease
- Talk:Major histocompatibility complex, class II, DQ alpha 1
- Talk:Malignant hyperthermia
- Talk:Malonic aciduria
- Talk:Maple syrup urine disease
- Talk:Marfan syndrome
- Talk:Marker chromosome
- Talk:Michelle Maykin
- Talk:McCune–Albright syndrome
- Talk:McLeod syndrome
- Talk:Medical genetics
- Talk:Medical genetics of Jews
- Talk:Medium-chain acyl-coenzyme A dehydrogenase deficiency
- Talk:Metachondromatosis
- Talk:Metachromatic leukodystrophy
- Talk:Methylmalonyl-CoA mutase deficiency
- Talk:Microcephalic primordial dwarfism, Montreal type
- Talk:Microcephaly
- Talk:Microchimerism
- Talk:Microcytic anemia
- Talk:Microdeletion syndrome
- Talk:Migraine
- Talk:Mild androgen insensitivity syndrome
- Talk:Miller–Dieker syndrome
- Talk:Minor physical anomalies
- Talk:Mismatch repair cancer syndrome
- Talk:Mitochondrial complex II deficiency
- Talk:Mitochondrial trifunctional protein deficiency
- Talk:Molybdenum cofactor deficiency
- Talk:MOMO syndrome
- Talk:Moonrise (Wolfson book)
- Talk:MORM syndrome
- Talk:D. Holmes Morton
- Talk:Mosaic loss of chromosome Y
- Talk:Roxana Moslehi
- Talk:Mouse models of Down syndrome
- Talk:MPI-CDG
- Talk:Mucolipidosis
- Talk:Mucopolysaccharidosis
- Talk:Mulibrey nanism
- Talk:Multifactorial disease
- Talk:Multiple endocrine neoplasia type 1
- Talk:Multiple endocrine neoplasia type 2
- Talk:Multiple sulfatase deficiency
- Talk:Muscular dystrophy
- Talk:Myelokathexis
- Talk:Myeloperoxidase deficiency
- Talk:Myopathy
- Talk:Myotonia congenita
- Talk:Myotonic dystrophy