Category:Low-importance medical genetics articles
 | Administrators: Please do not delete this category as empty! This category may be empty occasionally or even most of the time. |
| Top | High | Mid | Low | NA | ??? |
| 4 | 27 | 90 | 238 | 189 | 712 |
Pages in category "Low-importance medical genetics articles"
The following 152 pages are in this category, out of approximately 238 total. This list may not reflect recent changes.
(previous page) (next page)F
- Talk:Faciocardiorenal syndrome
- Talk:FAD-dependent oxidoreductase domain-containing protein 2
- 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: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:Gamma-aminobutyric acid receptor-associated protein-like 1
- 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
- Talk:Mitchell Guttman
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:Protein zyg-11 homolog A
- Talk:Proud syndrome
- Talk:Pubmeth
- Talk:PURA syndrome
- Talk:Pyknoachondrogenesis
R
S
- Talk:Nadia Awni Sakati
- Talk:Savior sibling
- Talk:Say-Field-Coldwell syndrome
- Talk:Selenium in biology
- Talk:Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
- Talk:Serrated polyposis syndrome
- Talk:Single umbilical artery
- Talk:Sonoda syndrome
- Talk:Spinal muscular atrophy with lower extremity predominance 2A
- Talk:Spondylocamptodactyly
- Talk:Spondyloepimetaphyseal dysplasia-short limb-abnormal calcification syndrome
- Talk:St. Helena familial genu valgum
- Talk:Stocco dos Santos syndrome