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Disease	Synonyms	Description	Articles	Phenotypes
salivary gland carcinoma		A salivary gland cancer that has_material_basis_in..[+] A salivary gland cancer that has_material_basis_in epithelial cells. [-]
spindle epithelial tumor with thymus-like differentiation tumor	spindle epithelial tumour with thymus-like differe.. [+] spindle epithelial tumour with thymus-like differentiation tumour; SETTLE tumour; SETTLE tumor [-]	A thyroid gland carcinoma that has_material_basis_..[+] A thyroid gland carcinoma that has_material_basis_in compact bundles of long spindle epithelial cells that merge with tubulopapillary structures and/or mucinous glands. [-]
striated muscle rhabdoid tumor		A muscle cancer that is located_in striated muscle..[+] A muscle cancer that is located_in striated muscle and has_material_basis_in rhabdoid cells which are large cells with eccentrically located nuclei and abundant, eosinophilic cytoplasm. [-]
small intestine carcinoid neuroendocrine tumor	'intestinal carcinoid tumour'; intestinal carcinoi.. [+] 'intestinal carcinoid tumour'; intestinal carcinoid tumour [-]	A neuroendocrine tumor that has_material_basis_in ..[+] A neuroendocrine tumor that has_material_basis_in cells of the neuroendocrine system and that is located in the small intestine. [-]
sublingual gland adenoid cystic carcinoma		A sublingual gland cancer that is characterized by..[+] A sublingual gland cancer that is characterized by a distinctive pattern in which abnormal nests or cords of epithelial cells surround and/or infiltrate ducts or glandular structures within the affected organ. [-]
spastic ataxia 2		A spastic ataxia that is characterized by cerebell..[+] A spastic ataxia that is characterized by cerebellar ataxia, spasticity and peripheral neuropathy in the first two decades of life, has_material_basis_in homozygous mutation in the KIF1C gene on chromosome 17p13. [-]
spastic ataxia 3		A spastic ataxia that is characterized by cerebell..[+] A spastic ataxia that is characterized by cerebellar ataxia, spasticity, hyperreflexia, urinary urgency and dysarthria, has_material_basis_in homozygous or compound heterozygous complex genomic rearrangements involving the MARS2 gene on chromosome 2q33. [-]
spastic ataxia 4		A spastic ataxia that is characterized by cerebell..[+] A spastic ataxia that is characterized by cerebellar ataxia, spasticity, dysarthria and optic atrophy, has_material_basis_in homozygous mutation in the MTPAP gene on chromosome 10p11. [-]
spastic ataxia 5		n_a
spastic ataxia 7		A spastic ataxia that is characterized by poor vis..[+] A spastic ataxia that is characterized by poor visual acuity, cerebellar ataxia, dysarthria and pyramidal signs. [-]
spastic ataxia		A hereditary ataxia that is characterized by early..[+] A hereditary ataxia that is characterized by early onset of cerebellar ataxia, pyramidal tract signs and peripheral neuropathy. [-]
spinocerebellar ataxia type 1		An autosomal dominant cerebellar ataxia that is ch..[+] An autosomal dominant cerebellar ataxia that is characterized by ataxia, dysarthria, dysphagia, dystonia and peripheral neuropathy that begins in early adulthood, has_material_basis_in the expanded (CAG)n trinucleotide repeat of ataxin-1 gene on chromosome 6p22. [-]	1 articles
spinocerebellar ataxia type 2		n_a
spinocerebellar ataxia type 6		An autosomal dominant cerebellar ataxia that is ch..[+] An autosomal dominant cerebellar ataxia that is characterized by progresive ataxia, has_material_basis_in mutation in the CACNA1A gene. [-]
spinocerebellar ataxia type 4		An autosomal dominant cerebellar ataxia that is ch..[+] An autosomal dominant cerebellar ataxia that is characterized by progresive ataxia, dysarthria and peripheral neuropathy, has_material_basis_in mutation in the SCA4 gene. [-]
spinocerebellar ataxia type 7		n_a
spinocerebellar ataxia type 8		n_a
spinocerebellar ataxia type 10		An autosomal dominant cerebellar ataxia that is ch..[+] An autosomal dominant cerebellar ataxia that is characterized by gait ataxia, upper-limb ataxia, dysarthria and dysphagia, has_material_basis_in mutation in the ATXN10 gene. [-]
spinocerebellar ataxia type 11		An autosomal dominant cerebellar ataxia that is ch..[+] An autosomal dominant cerebellar ataxia that is characterized by ataxia, nystagmus, pyramidal abnormalities and peripheral neuropathy, has_material_basis_in mutation in the TTBK2 gene. [-]
spinocerebellar ataxia type 12		n_a
spinocerebellar ataxia type 13		n_a
spinocerebellar ataxia type 14		n_a
spinocerebellar ataxia type 15		n_a
spinocerebellar ataxia type 16		n_a
spinocerebellar ataxia type 17		An autosomal dominant cerebellar ataxia that is ch..[+] An autosomal dominant cerebellar ataxia that is characterized by chorea, dementia, dystonia, spasiticity and seizure, has_material_basis_in CAG repeat expansion in the TBP gene. [-]
spinocerebellar ataxia type 18		An autosomal dominant cerebellar ataxia that is ch..[+] An autosomal dominant cerebellar ataxia that is characterized by cerebellar ataxia and sensory neuropathy, has_material_basis_in mutation on chromosome 7q22-q23. [-]
spinocerebellar ataxia type 19/22		An autosomal dominant cerebellar ataxia that is ch..[+] An autosomal dominant cerebellar ataxia that is characterized by mild cerebellar ataxia, cognitive impairment, myoclonus and tremor. [-]
spinocerebellar ataxia type 20		An autosomal dominant cerebellar ataxia that is ch..[+] An autosomal dominant cerebellar ataxia that is characterized by cerebellar dysarthria. [-]
spinocerebellar ataxia type 21		An autosomal dominant cerebellar ataxia that is ch..[+] An autosomal dominant cerebellar ataxia that is characterized by progressive cerebellar ataxia, cognitive impairment, tremor, bradykinesia and rigidity. [-]
spinocerebellar ataxia type 23		n_a
spinocerebellar ataxia type 25		An autosomal dominant cerebellar ataxia that is ch..[+] An autosomal dominant cerebellar ataxia that is characterized by ataxia and sensory neuropathy, has_material_basis_in repeat CAG expansion on chromosome 2p15-p21. [-]
spinocerebellar ataxia type 26		An autosomal dominant cerebellar ataxia that is ch..[+] An autosomal dominant cerebellar ataxia that is characterized by slowly progressive ataxia and oculomotor abnormalities, has_material_basis_in mutation in the EEF2 gene. [-]
spinocerebellar ataxia type 27	autosomal dominant congenital nystagmus 4; congeni.. [+] autosomal dominant congenital nystagmus 4; congenital nystagmus 4; vestibulocerebellar disorder with predominant ocular signs [-]	An autosomal dominant cerebellar ataxia that is ch..[+] An autosomal dominant cerebellar ataxia that is characterized by slowly progressive ataxia, early-onset tremor and dyskinesia, and has_material_basis_in heterozygous mutation in the FGF14 gene on chromosome 13q33. Some patients have heterozygous deletions of chromosome 13q33 affecting the FGF14 and ITGBL1 genes, which may thus be considered a contiguous gene deletion syndrome. [-]
spinocerebellar ataxia type 28		n_a
spinocerebellar ataxia type 29		n_a
spinocerebellar ataxia type 30		An autosomal dominant cerebellar ataxia that is ch..[+] An autosomal dominant cerebellar ataxia that is characterized by slowly progressive gait abnormalities and dysarthria, has_material_basis_in mutation in the ODZ3 gene. [-]
spinocerebellar ataxia type 31		n_a
spinocerebellar ataxia type 34		n_a
spinocerebellar ataxia type 35		n_a
spinocerebellar ataxia type 36		n_a
spinocerebellar ataxia type 37		n_a
spinocerebellar ataxia type 38		n_a
spinocerebellar ataxia type 40		An autosomal dominant cerebellar ataxia that is ch..[+] An autosomal dominant cerebellar ataxia that is characterized by progressive gait abnormalities, dysarthria, tremor and hyporeflexia, has_material_basis_in mutation in the CCDC88C gene. [-]
specific developmental disorder		A developmental disorder of mental health that cat..[+] A developmental disorder of mental health that categorizes specific learning disabilities and developmental disorders affecting coordination. [-]	48 articles	54 matches
sexual health disorder		A disease of mental health that involves the impai..[+] A disease of mental health that involves the impairment in normal sexual functioning. [-]	1 articles
sideroblastic anemia 1	sideroblastic anaemia 1; XLSA; X-linked sideroblas.. [+] sideroblastic anaemia 1; XLSA; X-linked sideroblastic anaemia; X-linked sideroblastic anemia [-]	A sideoblastic anemia that is characterized by the..[+] A sideoblastic anemia that is characterized by the presence of microcytic hypochromic anemia and iron overload, and has_material_basis_in X-linked inheritance of mutation in the ALAS2 gene that enocdes aminolevulinic acid synthase that catalyzes the first step in heme production. [-]
sensory organ benign neoplasm		A nervous system benign neoplasm that is located_i..[+] A nervous system benign neoplasm that is located_in a sensory organ. [-]
sensory system cancer		A nervous system cancer that is located in the sen..[+] A nervous system cancer that is located in the sensory system. [-]	7 articles	25 matches
semantic agnosia		An agnosia that is a loss of the ability to visual..[+] An agnosia that is a loss of the ability to visually recognise an object while maintaining the use of non-visual sensory systems such as feeling, tapping, smelling, rocking or flicking the object to recognise the object. [-]
simultanagnosia		An agnosia that is a loss of the ability to recgon..[+] An agnosia that is a loss of the ability to recgonize a whole image or scene while retianing the ability to recognize objects or details in their visual field one at a time. [-]

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