Category:Genetic diseases and disorders
From HandWiki
Here is a list of articles in the category Genetic diseases and disorders of the Medicine portal.
Subcategories
This category has the following 2 subcategories, out of 2 total.
Pages in category "Genetic diseases and disorders"
The following 71 pages are in this category, out of 210 total.
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P
- Medicine:Pantothenate kinase-associated neurodegeneration
- Medicine:Paroxysmal nonkinesigenic dyskinesia
- Medicine:Pascual-Castroviejo syndrome
- Medicine:PASLI disease
- Medicine:PGM3 deficiency
- Medicine:Plum syndrome
- Medicine:PMM2 deficiency
- Medicine:Polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy
- Medicine:Primordial dwarfism
R
- Medicine:Rare functional variant
- Medicine:Rare variant (genetics)
- Medicine:RAS-associated autoimmune leukoproliferative disorder
- Medicine:Reparagen
- Medicine:Retinal cone dystrophy 3B
- Medicine:Rhizomelic dysplasia, scoliosis, and retinitis pigmentosa
- Medicine:Ring 18
- Medicine:Ring chromosome 18
- Medicine:Ring chromosome 20
- Biology:RNA-dominant disease
S
- Medicine:Saito-Kuba-Tsuruta syndrome
- Medicine:Santos-Mateus-Leal syndrome
- Medicine:Sclerosteosis
- Medicine:Sensory ataxic neuropathy, dysarthria, and ophthalmoparesis
- Medicine:Serkal syndrome
- Biology:Shaker (gene)
- Biology:Shaker gene
- Medicine:Short-limb skeletal dysplasia with severe combined immunodeficiency
- Medicine:SLC35A1-CDG
- Medicine:Snijders Blok-Campeau syndrome
- Medicine:Sorsby's fundus dystrophy
- Medicine:Spastin
- Medicine:Spinal muscular atrophies
- Medicine:Sponastrime dysplasia
- Medicine:Spondylocamptodactyly
- Medicine:Spondylometaphyseal dysplasia, East-African type
- Medicine:St. Helena familial genu valgum
- Medicine:STAT3 GOF
- Medicine:STING-associated vasculopathy with onset in infancy
- Medicine:Swedish mutation
- Medicine:SYNGAP1-related intellectual disability
- Medicine:SYT1-associated neurodevelopmental disorder