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Pages in category "Low-importance medical genetics articles"
The following 200 pages are in this category, out of approximately 226 total. This list may not reflect recent changes.
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A
- Talk:Aase syndrome
- Talk:Abderhalden–Kaufmann–Lignac syndrome
- Talk:Ablepharon macrostomia syndrome
- Talk:Absence deformity of leg-cataract syndrome
- Talk:Acro-oto-radial syndrome
- Talk:Acrocraniofacial dysostosis
- Talk:Acute fatty liver of pregnancy
- Talk:Adams–Oliver syndrome
- Talk:Advanced Therapy Medicinal Product
- Talk:African Centre of Excellence for Genomics of Infectious Diseases
- Talk:Aicardi–Goutières syndrome
- Talk:Al Gazali Sabrinathan Nair syndrome
- Talk:Alpha-1 antitrypsin deficiency
- Talk:Alport syndrome
- Talk:Amaurosis congenita, cone-rod type, with congenital hypertrichosis
- Talk:Amish lethal microcephaly
- Talk:Anonychia-onychodystrophy with brachydactyly type B and ectrodactyly
- Talk:Armed Forces DNA Identification Laboratory
- Talk:Aromatase deficiency
- Talk:Hans Asperger
- Talk:Autism and memory
- Talk:Autophagic vacuolar myopathy
- Talk:Autosomal dominant cerebellar ataxia, deafness, and narcolepsy
- Talk:Autosomal dominant porencephaly type I
B
- Talk:Background radiation equivalent time
- Talk:Bartter syndrome
- Talk:BeiGene
- Talk:Benign familial infantile epilepsy
- Talk:Biliary atresia
- Talk:Blepharophimosis intellectual disability syndromes
- Talk:Blepharophimosis-ptosis-esotropia-syndactyly-short stature syndrome
- Talk:Boudhina-Yedes-Khiari syndrome
- Talk:Brachial amelia, cleft lip, and holoprosencephaly
- Talk:Brachydactyly-long thumb syndrome
- Talk:British Heart Foundation
- Talk:Broad Institute
C
- Talk:Camera–Marugo–Cohen syndrome
- Talk:Camptodactyly-arthropathy-coxa vara-pericarditis syndrome
- Talk:Cataract-ataxia-deafness syndrome
- Talk:CDKL5 deficiency disorder
- Talk:Celera Corporation
- Talk:Cerebellar ataxia, neuropathy, vestibular areflexia syndrome
- Talk:Cerebro-costo-mandibular syndrome
- Talk:Chondrodysplasia, Grebe type
- Talk:Chudley–Mccullough syndrome
- Talk:Coeliac UK
- Talk:Congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency
- Talk:Congenital adrenal hyperplasia due to 11β-hydroxylase deficiency
- Talk:Congenital muscular dystrophy-infantile cataract-hypogonadism syndrome
- Talk:Congenital pulmonary airway malformation
- Talk:Congenital tufting enteropathy
- Talk:Conorenal syndrome
- Talk:Cornea plana 1
- Talk:Cornea plana 2
- Talk:Cryptorchidism-arachnodactyly-intellectual disability syndrome
- Talk:Cryptotia
D
- Talk:Dauwerse–Peters syndrome
- Talk:Deafness-vitiligo-achalasia syndrome
- Talk:Dent's disease
- Talk:Denys–Drash syndrome
- Talk:Dihydrofolate reductase deficiency
- Talk:Dihydropteridine reductase deficiency
- Talk:Distal intestinal obstruction syndrome
- Talk:DNA digital data storage
- Talk:Du Pan syndrome
- Talk:Duane syndrome
- Talk:Dup15q
- Talk:Dwarfism, low-birth-weight type with unresponsiveness to growth hormone
F
- Talk:Faciocardiorenal syndrome
- Talk:Familial dwarfism and painful muscle spasms
- Talk:Familial multiple cafe-au-lait spots
- Talk:Familial nasal acilia
- Talk:Familial osteodysplasia, Anderson type
- Talk:Alessio Fasano
- Talk:FBXW7 neurodevelopmental syndrome
- Talk:Feigenbaum-Bergeron-Richardson syndrome
- Talk:Feingold syndrome
- Talk:David S. Feldman
- Talk:FG syndrome
- Talk:Fibular aplasia-ectrodactyly syndrome
- Talk:Fragile X syndrome
- Talk:Kelly A. Frazer
- Talk:Brendan Frey
- Talk:Fryns syndrome
G
- Talk:Galactosemia
- Talk:Garrod's tetrad
- Talk:GATAD2B-associated neurodevelopmental disorder
- Talk:Genes, Brain and Behavior
- Talk:Genodermatosis
- Talk:Gitelman syndrome
- Talk:Glycogen storage disease type IX
- Talk:Glycogen storage disease type VI
- Talk:GM2-gangliosidosis, AB variant
- Talk:GNE (gene)
- Talk:Growth delay-hydrocephaly-lung hypoplasia syndrome
H
- Talk:Halperin-Birk syndrome
- Talk:Healthcare scientist
- Talk:Heart-hand syndrome, Spanish type
- Talk:Heimler syndrome
- Talk:Hemimelia
- Talk:Hennekam syndrome
- Talk:Hereditary cystatin C amyloid angiopathy
- Talk:Hereditary haemochromatosis
- Talk:Hereditary lobular breast cancer
- Talk:Hereditary pancreatitis
- Talk:Hereditary stomatocytosis
- Talk:Hirschsprung's disease
- Talk:Hirschsprung's disease-type D brachydactyly syndrome
- Talk:History of Tay–Sachs disease
- Talk:Niels Høiby
- Talk:Human disease modifier gene
- Talk:Human Heredity and Health in Africa
- Talk:Huntington's disease clinical research
- Talk:HUPRA syndrome
- Talk:Hypotrichosis with juvenile macular dystrophy
I
L
M
- Talk:Mandibulofacial dysostosis-microcephaly syndrome
- Talk:Marinesco-Sjogren syndrome
- Talk:McGillivray syndrome
- Talk:Meacham syndrome
- Talk:Microcephaly deafness syndrome
- Talk:Mir-390 microRNA precursor family
- Talk:Mir-590 microRNA precursor family
- Talk:Mir-618 microRNA precursor family
- Talk:Mir-624 microRNA precursor family
- Talk:Mir-625 microRNA precursor family
- Talk:Mir-633 microRNA precursor family
- Talk:Mir-636 microRNA precursor family
- Talk:Mir-638 microRNA precursor family
- Talk:Mir-650 microRNA precursor family
- Talk:Mir-652 microRNA precursor family
- Talk:Mir-663 microRNA precursor family
- Talk:Mir-708 microRNA precursor family
- Talk:Mir-711 microRNA precursor family
- Talk:Mir-3180 microRNA precursor family
- Talk:Missing heritability problem
- Talk:Mitochondrial biogenesis
- Talk:Moebius syndrome
- Talk:Molecular risk assessment
- Talk:Mongolian idiocy
- Talk:Multifocal stenosing ulceration of the small intestine
- Talk:Multiple congenital anomalies-hypotonia-seizures syndrome
- Talk:Muscular Dystrophy Association
- Talk:MUTYH-associated polyposis
- Talk:Myopathy, X-linked, with excessive autophagy
N
P
- Talk:Pancreaticobiliary maljunction
- Talk:PANO1
- Talk:Papillorenal syndrome
- Talk:Polydactyly-myopia syndrome
- Talk:Polymerase proofreading-associated polyposis
- Talk:Potocki–Shaffer syndrome
- Talk:Prime editing
- Talk:Progerin
- Talk:Progressive cardiac conduction defect
- Talk:Progressive pseudorheumatoid dysplasia
- Talk:Proud syndrome
- Talk:Pubmeth
- Talk:PURA syndrome
- Talk:Pyknoachondrogenesis