Category:B-Class medical genetics articles
 | Administrators: Please do not delete this category as empty! This category may be empty occasionally or even most of the time. |
 FA |  A |  GA | B | C | Start | Stub | FL | List | Category | Disambig | FM | Project | Redirect | Template | NA | ??? | Total |
| 3 | 0 | 23 | 159 | 288 | 435 | 149 | 0 | 11 | 82 | 2 | 1 | 4 | 90 | 1 | 0 | 0 | 1,248 |
Pages in category "B-Class medical genetics articles"
The following 159 pages are in this category, out of 159 total. This list may not reflect recent changes.
0–9
A
- Talk:Aceruloplasminemia
- Talk:Achondroplasia
- Talk:Achromatopsia
- Talk:Acrodermatitis enteropathica
- Talk:Acute fatty liver of pregnancy
- Talk:Adenine phosphoribosyltransferase deficiency
- Talk:Adenosine deaminase 2 deficiency
- Talk:Adenosine deaminase deficiency
- Talk:Adrenoleukodystrophy
- Talk:Aicardi syndrome
- Talk:Alexander disease
- Talk:Alpha-mannosidosis
- Talk:Alport syndrome
- Talk:Androgen insensitivity syndrome
- Talk:Aneuploidy
- Talk:Angelman syndrome
- Talk:Aromatase deficiency
- Talk:Asperger syndrome
- Talk:Ataxia–telangiectasia
- Talk:Autism
- Talk:Autosomal dominant polycystic kidney disease
C
- Talk:CDKL5 deficiency disorder
- Talk:Cell-free fetal DNA
- Talk:Cerebrotendinous xanthomatosis
- Talk:Childhood absence epilepsy
- Talk:Color blindness
- Talk:Complete androgen insensitivity syndrome
- Talk:Congenital adrenal hyperplasia
- Talk:Congenital adrenal hyperplasia due to 3β-hydroxysteroid dehydrogenase deficiency
- Talk:Congenital adrenal hyperplasia due to 21-hydroxylase deficiency
- Talk:Congenital athymia
- Talk:Congenital disorder of glycosylation
- Talk:Congenital hyperinsulinism
- Talk:Congenital muscular dystrophy
- Talk:Copper in biology
- Talk:Copy number variation
- Talk:CRISPR gene editing
- Talk:Cystic fibrosis
- Talk:Cystic fibrosis transmembrane conductance regulator
- Talk:Cytogenetics
E
F
G
- Talk:Gaucher's disease
- Talk:Gene delivery
- Talk:Gene therapy
- Talk:Gene therapy for osteoarthritis
- Talk:Genetic disorder
- Talk:Genetic linkage
- Talk:Genetic testing
- Talk:Genetics of Down syndrome
- Talk:Genomic imprinting
- Talk:Genomics
- Talk:Germline mutation
- Talk:Gitelman syndrome
- Talk:Generalized glucocorticoid resistance
- Talk:Glutaric aciduria type 1
- Talk:Gluten immunochemistry
- Talk:GM2-gangliosidosis, AB variant
- Talk:Gulf War syndrome
H
L
M
N
P
- Talk:Papillorenal syndrome
- Talk:Partial androgen insensitivity syndrome
- Talk:Pattern hair loss
- Talk:Pectus excavatum
- Talk:Personal genomics
- Talk:Personalized medicine
- Talk:Pharmacogenomics
- Talk:Phenylketonuria
- Talk:Pioneer Fund
- Talk:Plasmodium falciparum erythrocyte membrane protein 1
- Talk:Porphyria
- Talk:Prader–Willi syndrome
- Talk:Preimplantation genetic diagnosis
- Talk:Prime editing
- Talk:Progeria
- Talk:Progeroid syndromes
- Talk:Public health genomics
- Talk:Pyloric stenosis