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 693 total. This list may not reflect recent changes.
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- Talk:CADASIL
- Talk:Camptodactyly
- Talk:Camptodactyly-taurinuria syndrome
- Talk:Canavan disease
- Talk:Carbamoyl phosphate synthetase I deficiency
- Talk:Cardiofaciocutaneous syndrome
- Talk:Carnitine palmitoyltransferase I deficiency
- Talk:Carnitine palmitoyltransferase II deficiency
- Talk:Carnitine-acylcarnitine translocase deficiency
- Talk:Carpenter syndrome
- Talk:Carrier testing
- Talk:Cat eye syndrome
- Talk:Causes of autism
- Talk:CCR2
- Talk:CCR5
- Talk:Central nervous system cavernous hemangioma
- Talk:CHAMP1-associated intellectual disability syndrome
- Talk:Channelopathy
- Talk:CHCHD10
- Talk:Childhood absence epilepsy
- Talk:Chorionic villus sampling
- Talk:Chromosome 1
- Talk:Chromosome 2
- Talk:Chromosome 3
- Talk:Chromosome 4
- Talk:Chromosome 5
- Talk:Chromosome 5q deletion syndrome
- Talk:Chromosome 10
- Talk:Chromosome 11
- Talk:Chromosome 14
- Talk:Chromosome 15q partial deletion
- Talk:Chromosome 15q trisomy
- Talk:Chromosome 17
- Talk:Chromosome 18
- Talk:Chromosome 20
- Talk:Chromosome 21
- Talk:Chromosome 22
- Talk:Chromosome abnormality
- Talk:Chromosome instability
- Talk:Chromosome instability syndrome
- Talk:Chronic granulomatous disease
- Talk:Ciliopathy
- Talk:Citrullinemia
- Talk:Cleft palate short stature vertebral anomalies syndrome
- Talk:Clinic for Special Children
- Talk:Clinodactyly
- Talk:Cockayne syndrome
- Talk:Codon degeneracy
- Talk:Coffin–Lowry syndrome
- Talk:Cohen syndrome
- Talk:Collagenopathy, types II and XI
- Talk:Color blindness
- Talk:Complete androgen insensitivity syndrome
- Talk:Complex segregation analysis
- Talk:Compound heterozygosity
- Talk:Congenital adrenal hyperplasia
- Talk:Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- Talk:Congenital disorder of glycosylation
- Talk:Congenital disorder of glycosylation type IIc
- Talk:Congenital distal spinal muscular atrophy
- Talk:Congenital dyserythropoietic anemia type I
- Talk:Congenital dyserythropoietic anemia type II
- Talk:Congenital dyserythropoietic anemia type III
- Talk:Congenital dyserythropoietic anemia type IV
- Talk:Congenital hyperinsulinism
- Talk:Congenital muscular dystrophy
- Talk:Contiguous gene syndrome
- Talk:Copy number variation
- Talk:Coronary artery anomaly
- Talk:Costello syndrome
- Talk:Cousin syndrome
- Talk:Craniodiaphyseal dysplasia
- Talk:Cri du chat syndrome
- Talk:Crigler–Najjar syndrome
- Talk:Crisscross heart
- Talk:Crohn's disease
- Talk:Crouzon syndrome
- Talk:Crouzonodermoskeletal syndrome
- Talk:Cystinosis
- Talk:Cystinuria
- Talk:Cytogenetics
D
- Talk:De Barsy syndrome
- Talk:De Finetti diagram
- Talk:DeFries–Fulker regression
- Talk:Deletion (genetics)
- Talk:Dentinogenesis imperfecta
- Talk:Developmental coordination disorder
- Talk:Dextrocardia
- Talk:Diagnosis of autism
- Talk:Diagnostic Interview for Genetic Studies
- Talk:Diamond–Blackfan anemia
- Talk:Diastrophic dysplasia
- Talk:DiGeorge syndrome
- Talk:Dihydropyrimidine dehydrogenase deficiency
- Talk:Distal hereditary motor neuronopathies
- Talk:Distal trisomy 10q
- Talk:DNA repair-deficiency disorder
- Talk:Dolichonychia
- Talk:DOOR syndrome
- Talk:Dor Yeshorim
- Talk:Down syndrome
- Talk:Duane-radial ray syndrome
- Talk:Duchenne muscular dystrophy
- Talk:Dystrophin
E
- Talk:Ectrodactyly
- Talk:Ehlers–Danlos syndrome
- Talk:Ellis–Van Creveld syndrome
- Talk:Emery–Dreifuss muscular dystrophy
- Talk:Emily's Entourage
- Talk:Epidemiology of autism
- Talk:Epidermolysis bullosa
- Talk:Epidermolytic hyperkeratosis
- Talk:Epigenetics of anxiety and stress–related disorders
- Talk:Epigenetics of autoimmune disorders
- Talk:Erythromelalgia
- Talk:Erythropoiesis
- Talk:Erythropoietic protoporphyria
- Talk:Ethylmalonic encephalopathy
- Talk:Expression quantitative trait loci
- Talk:Expressivity (genetics)
F
- Talk:Fabry disease
- Talk:Facioscapulohumeral muscular dystrophy
- Talk:Factor IX
- Talk:Factor V Leiden
- Talk:Factor VIII
- Talk:Factor XI
- Talk:Familial adenomatous polyposis
- Talk:Familial amyloid polyneuropathy
- Talk:Familial dysautonomia
- Talk:Familial episodic pain syndrome
- Talk:Familial hemiplegic migraine
- Talk:Familial isolated vitamin E deficiency
- Talk:Familial Mediterranean fever
- Talk:Familial opposable triphalangeal thumbs duplication
- Talk:Familial thoracic aortic aneurysm and aortic dissection
- Talk:Fanconi anemia
- Talk:Fazio–Londe disease
- Talk:Fetal hydantoin syndrome
- Talk:Fibular hemimelia
- Talk:Fine–Lubinsky syndrome
- Talk:Floating–Harbor syndrome
- Talk:Flynn–Aird syndrome
- Talk:JoAnne Flynn
- Talk:Focal facial dermal dysplasia
- Talk:Fraser syndrome
- Talk:Frasier syndrome
- Talk:Frontotemporal dementia and parkinsonism linked to chromosome 17
- Talk:Fructose malabsorption
- Talk:Fukuyama congenital muscular dystrophy
G
- 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