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 692 total. This list may not reflect recent changes.
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- Talk:1p36 deletion syndrome
- Talk:2-Hydroxyglutaric aciduria
- Talk:2-Methylbutyryl-CoA dehydrogenase deficiency
- Talk:2,4 Dienoyl-CoA reductase deficiency
- Talk:2p15-16.1 microdeletion syndrome
- Talk:2q37 deletion syndrome
- Talk:3 hydroxyisobutyric aciduria
- Talk:3-Hydroxy-3-methylglutaryl-CoA lyase deficiency
- Talk:3-Hydroxyisobutyryl-CoA deacylase deficiency
- Talk:3-Methylcrotonyl-CoA carboxylase deficiency
- Talk:3-Methylglutaconic aciduria
- Talk:6-phosphogluconate dehydrogenase deficiency
- Talk:6-Pyruvoyltetrahydropterin synthase deficiency
- Talk:7q11.23 duplication syndrome
- Talk:13q deletion syndrome
- Talk:22q11.2 distal deletion syndrome
- Talk:22q11.2 duplication syndrome
- Talk:22q13 deletion syndrome
- Talk:45,X/46,XY mosaicism
- Talk:46,XX/46,XY
A
- Talk:Aagenaes syndrome
- Talk:ABCB5
- Talk:ABCD syndrome
- Talk:Abetalipoproteinemia
- Talk:Acatalasia
- Talk:Aceruloplasminemia
- Talk:Achondrogenesis
- Talk:Achondrogenesis type 1B
- Talk:Achondrogenesis type 2
- Talk:Achondroplasia
- Talk:Achondroplasia in children
- Talk:Achromatopsia
- Talk:Acorea, microphthalmia and cataract syndrome
- Talk:Acrodermatitis enteropathica
- Talk:Acrokeratosis verruciformis
- Talk:Acute necrotizing encephalopathy
- Talk:Acyl-CoA oxidase deficiency
- Talk:Adducted thumb syndrome
- Talk:Adenine phosphoribosyltransferase deficiency
- Talk:Adenosine deaminase 2 deficiency
- Talk:Adenosine deaminase deficiency
- Talk:Adenylosuccinate lyase deficiency
- Talk:Adermatoglyphia
- Talk:Adrenoleukodystrophy
- Talk:African iron overload
- Talk:Agammaglobulinemia-microcephaly-craniosynostosis-severe dermatitis syndrome
- Talk:AHDC1
- Talk:Aicardi syndrome
- Talk:Alagille syndrome
- Talk:Alder–Reilly anomaly
- Talk:Aldolase A deficiency
- Talk:Alexander disease
- Talk:ALG1-CDG
- Talk:Alkaptonuria
- Talk:Allelic heterogeneity
- Talk:Alpha-mannosidosis
- Talk:Alström syndrome
- Talk:Alternating hemiplegia of childhood
- Talk:Amelogenesis imperfecta
- Talk:Aminoacylase 1 deficiency
- Talk:Andersen–Tawil syndrome
- Talk:Androgen insensitivity syndrome
- Talk:Aneuploidy
- Talk:Angel-shaped phalango-epiphyseal dysplasia
- Talk:Angelman syndrome
- Talk:Antagonistic pleiotropy hypothesis
- Talk:Anticipation (genetics)
- Talk:Aortic arch anomaly - peculiar facies - intellectual disability
- Talk:Aortopulmonary septal defect
- Talk:Apert syndrome
- Talk:Aphalangy-syndactyly-microcephaly syndrome
- Talk:Apparent mineralocorticoid excess syndrome
- Talk:Arakawa's syndrome II
- Talk:Argininosuccinic aciduria
- Talk:Asymmetric crying facies
- Talk:Ataxia–telangiectasia
- Talk:Atelosteogenesis, type II
- Talk:Athabaskan brainstem dysgenesis syndrome
- Talk:ATR-16 syndrome
- Talk:ATR-X syndrome
- Talk:Autism: The Musical
- Talk:Autosomal dominant cerebellar ataxia
- Talk:Autosomal dominant intellectual disability-craniofacial anomalies-cardiac defects syndrome
- Talk:Autosomal dominant polycystic kidney disease
- Talk:Autosomal recessive multiple epiphyseal dysplasia
B
- Talk:Bainbridge–Ropers syndrome
- Talk:Baller–Gerold syndrome
- Talk:Bannayan–Riley–Ruvalcaba syndrome
- Talk:Banti's syndrome
- Talk:Barakat-Perenthaler syndrome
- Talk:Bardet–Biedl syndrome
- Talk:Bare lymphocyte syndrome
- Talk:Bare lymphocyte syndrome type II
- Talk:Barth syndrome
- Talk:Bazex–Dupré–Christol syndrome
- Talk:Becker muscular dystrophy
- Talk:Beckwith–Wiedemann syndrome
- Talk:Behavioural genetics
- Talk:Behr syndrome
- Talk:Benign hereditary chorea
- Talk:Berdon syndrome
- Talk:Beta-ketothiolase deficiency
- Talk:Binder's syndrome
- Talk:Biotinidase
- Talk:Biotinidase deficiency
- Talk:Birt–Hogg–Dubé syndrome
- Talk:Bloom syndrome
- Talk:Blue diaper syndrome
- Talk:Bochdalek hernia
- Talk:Bosch–Boonstra–Schaaf optic atrophy syndrome
- Talk:Brody myopathy
- Talk:Brown–Vialetto–Van Laere syndrome
- Talk:Brugada syndrome
- Talk:Ed Byrne (neuroscientist)
C
- 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