Disease Index
9,486 diseasesautosomal recessive spastic paraplegia type 66
human disease
autosomal recessive spastic paraplegia type 67
human disease
autosomal recessive spastic paraplegia type 68
human disease
autosomal recessive spastic paraplegia type 69
human disease
autosomal recessive spastic paraplegia type 70
human disease
autosomal recessive spastic paraplegia type 71
human disease
autosomal recessive spastic paraplegia type 76
hereditary spastic paraplegia that has material basis in mutation in the CAPN1 gene on chromosome 11q13
autosomal recessive spinocerebellar ataxia 10
human disease
autosomal recessive spinocerebellar ataxia 11
human disease
autosomal recessive spinocerebellar ataxia 12
human disease
autosomal recessive spinocerebellar ataxia 13
Human disease
autosomal recessive spinocerebellar ataxia 14
Human disease
autosomal recessive spinocerebellar ataxia 15
human disease
autosomal recessive spinocerebellar ataxia 16
human disease
autosomal recessive spinocerebellar ataxia 17
human disease
autosomal recessive spinocerebellar ataxia 18
Human disease
autosomal recessive spinocerebellar ataxia 19
human disease
autosomal recessive spinocerebellar ataxia 2
human disease
MeSH: C565865
autosomal recessive spinocerebellar ataxia 20
human disease
autosomal recessive spinocerebellar ataxia 7
Human disease
MeSH: C563753
autosomal recessive spondylocostal dysostosis
MeSH: C535781
autosomal recessive spondylometaphyseal dysplasia, Mégarbané type
human disease
MeSH: C567644
autosomal recessive Stickler syndrome
autosomal recessive syndromic cerebellar ataxia
human disease
autosomal semi-dominant severe lipodystrophic laminopathy
human disease
autosomal thrombocytopenia with normal platelets
human disease
autosomal trisomy
human disease
autosomal uniparental disomy
human disease
AUTS12
human disease
avascular necrosis of genetic origin
instance of avascular necrosis that is caused by a modification of the individual's genome