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:Kabuki syndrome
- Talk:Emil Kakkis
- Talk:Kallmann syndrome
- Talk:Karyotype
- Talk:Katz syndrome
- Talk:KBG syndrome
- Talk:KCNQ2 developmental and epileptic encephalopathy
- Talk:Kearns–Sayre syndrome
- Talk:Kindler syndrome
- Talk:Klinefelter syndrome
- Talk:Klippel–Feil syndrome
- Talk:Kniest dysplasia
- Talk:Koolen–De Vries syndrome
- Talk:Krabbe disease
L
- Talk:Lactose intolerance
- Talk:Langer–Giedion syndrome
- Talk:Laron syndrome
- Talk:Larsen syndrome
- Talk:Late onset congenital adrenal hyperplasia
- Talk:Laurence–Moon syndrome
- Talk:Leber's hereditary optic neuropathy
- Talk:Leigh syndrome
- Talk:Lethal white syndrome
- Talk:Leukocyte adhesion deficiency
- Talk:Leukocyte adhesion deficiency-1
- Talk:Leukoencephalopathy with vanishing white matter
- Talk:Li–Fraumeni syndrome
- Talk:Lipid storage disorder
- Talk:Lipoid congenital adrenal hyperplasia
- Talk:List of disorders included in newborn screening programs
- Talk:List of people with color blindness
- Talk:Loading control
- Talk:Loeys–Dietz syndrome
- Talk:Long-chain 3-hydroxyacyl-coenzyme A dehydrogenase deficiency
- Talk:Long-term nonprogressor
- Talk:Lysinuric protein intolerance
M
- Talk:Madelung's deformity
- Talk:Mahvash disease
- Talk:Major histocompatibility complex, class II, DQ alpha 1
- Talk:Malignant hyperthermia
- Talk:Malonic aciduria
- Talk:Maple syrup urine disease
- Talk:Marfan syndrome
- Talk:Marker chromosome
- Talk:Michelle Maykin
- Talk:McCune–Albright syndrome
- Talk:McLeod syndrome
- Talk:Medical genetics
- Talk:Medical genetics of Jews
- Talk:Medium-chain acyl-coenzyme A dehydrogenase deficiency
- Talk:Metachondromatosis
- Talk:Metachromatic leukodystrophy
- Talk:Methylmalonic acidemia with homocystinuria
- Talk:Methylmalonyl-CoA mutase deficiency
- Talk:Microcephalic primordial dwarfism, Montreal type
- Talk:Microcephaly
- Talk:Microchimerism
- Talk:Microcytic anemia
- Talk:Microdeletion syndrome
- Talk:Migraine
- Talk:Mild androgen insensitivity syndrome
- Talk:Miller–Dieker syndrome
- Talk:Minor physical anomalies
- Talk:Mismatch repair cancer syndrome
- Talk:Mitochondrial complex II deficiency
- Talk:Mitochondrial trifunctional protein deficiency
- Talk:Molybdenum cofactor deficiency
- Talk:MOMO syndrome
- Talk:Moonrise (Wolfson book)
- Talk:MORM syndrome
- Talk:D. Holmes Morton
- Talk:Mosaic loss of chromosome Y
- Talk:Roxana Moslehi
- Talk:Mouse models of Down syndrome
- Talk:MPI-CDG
- Talk:Mucolipidosis
- Talk:Mucopolysaccharidosis
- Talk:Mulibrey nanism
- Talk:Multifactorial disease
- Talk:Multiple endocrine neoplasia type 1
- Talk:Multiple endocrine neoplasia type 2
- Talk:Multiple sulfatase deficiency
- Talk:Muscular dystrophy
- Talk:Myelokathexis
- Talk:Myeloperoxidase deficiency
- Talk:Myopathy
- Talk:Myotonia congenita
- Talk:Myotonic dystrophy
N
- Talk:N-Acetylglutamate synthase deficiency
- Talk:Nail–patella syndrome
- Talk:Nance–Horan syndrome
- Talk:National Bleeding Disorders Foundation
- Talk:National Society of Genetic Counselors
- Talk:Nemaline myopathy
- Talk:Neonatal adrenoleukodystrophy
- Talk:Neonatal hemochromatosis
- Talk:Neonatal teeth
- Talk:Neurofibromatosis
- Talk:Neurofibromatosis type I
- Talk:Neurofibromatosis type II
- Talk:Neuropathy, ataxia, and retinitis pigmentosa
- Talk:Niemann–Pick disease
- Talk:Niemann–Pick disease type C
- Talk:Nijmegen breakage syndrome
- Talk:Nonsyndromic deafness
- Talk:Noonan syndrome
- Talk:Noonan syndrome with multiple lentigines
- Talk:Norrie disease
- Talk:Northern epilepsy syndrome
- Talk:Nuclear gene
- Talk:Nuclear sexing
- Talk:Nucleotide salvage
- Talk:Nullisomic
O
- Talk:Occipital horn syndrome
- Talk:Ocular albinism type 1
- Talk:Oculodentodigital dysplasia
- Talk:Oculopharyngeal muscular dystrophy
- Talk:Odontoma dysphagia syndrome
- Talk:Omenn syndrome
- Talk:Oncogene
- Talk:Ornithine aminotransferase deficiency
- Talk:Ornithine transcarbamylase deficiency
- Talk:Osimertinib
- Talk:OSLAM syndrome
- Talk:Osteogenesis imperfecta
- Talk:Osteopathia striata with cranial sclerosis
- Talk:Osteoporosis-pseudoglioma syndrome
- Talk:Oto-palato-digital syndrome
- Talk:Otospondylomegaepiphyseal dysplasia
P
- Talk:Pallister–Hall syndrome
- Talk:Pallister–Killian syndrome
- Talk:Paramutation
- Talk:Paramyotonia congenita
- Talk:Partial androgen insensitivity syndrome
- Talk:Pashayan syndrome
- Talk:Patau syndrome
- Talk:Paternal mtDNA transmission
- Talk:Pattern hair loss
- Talk:PEHO syndrome
- Talk:Pelizaeus–Merzbacher disease
- Talk:PELVIS syndrome
- Talk:Pendred syndrome
- Talk:Penetrance
- Talk:Pentasomy X
- Talk:List of people with Down syndrome
- Talk:Periodic paralysis
- Talk:Persistent Müllerian duct syndrome
- Talk:Personal genomics
- Talk:Personalized medicine
- Talk:Personalized onco-genomics
- Talk:Peters-plus syndrome
- Talk:Peutz–Jeghers syndrome
- Talk:Pfeiffer syndrome
- Talk:Pharmacogenomics
- Talk:Phenylketonuria
- Talk:Philadelphia chromosome
- Talk:Photic sneeze reflex
- Talk:Pierre Robin sequence
- Talk:Plasmodium falciparum erythrocyte membrane protein 1
- Talk:Platyspondylic lethal skeletal dysplasia, Torrance type
- Talk:Point-of-care genetic testing
- Talk:Polydactyly
- Talk:Pontocerebellar hypoplasia
- Talk:Popliteal pterygium syndrome
- Talk:Porphyria
- Talk:Porphyria cutanea tarda
- Talk:Prader–Willi syndrome
- Talk:Preimplantation genetic diagnosis
- Talk:Preimplantation genetic haplotyping
- Talk:PRICKLE1-related progressive myoclonus epilepsy with ataxia
- Talk:Primrose syndrome
- Talk:Proband
- Talk:Proboscis (anomaly)
- Talk:Progeria
- Talk:Progeroid syndromes
- Talk:Progressive familial intrahepatic cholestasis
- Talk:Propionic acidemia
- Talk:Prothrombin G20210A
- Talk:Pseudocholinesterase deficiency
- Talk:Pseudodeficiency alleles
- Talk:Public health genomics
- Talk:Pyloric stenosis
- Talk:Pyruvate kinase deficiency