Genes | GeDiPNet - Gene Disease Pathway & Associations

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12471 to 12480 of 15448 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
12471	6608	SMO	Smoothened, frizzled class receptor	CRJS, FZD11, Gx, PHLS, SMOH	Ameloblastoma, Basal cell carcinoma, Brain neoplasms, Congenital hypothalamic hamartoma syndrome, Curry-jones syndrome, Gastrointestinal stromal tumor, Hirschsprung disease, Female infertility, Promyelocytic leukemia, Medulloblastoma, Meningioma, Osteoarthritis, Skin neoplasms, Systemic lupus erythematosus, Winter shortland temple syndrome
12472	64093	SMOC1	SPARC related modular calcium binding 1	OAS	Anophthalmia, Atherosclerosis, Atrial fibrillation, Congenital malformation syndromes predominantly involving limbs, Klippel-trenaunay syndrome, Liver cirrhosis, Microphthalmia, Osteoporosis, Peripheral arterial disease, Rubinstein-taybi syndrome, Thrombocytopenia, Vacterl association, Waardenburg anophthalmia syndrome
12473	64094	SMOC2	SPARC related modular calcium binding 2	DTDP1, MST117, MSTP117, MSTP140, SMAP2, bA270C4A.1, bA37D8.1, dJ421D16.1	Alzheimer disease, Dentin dysplasia, Bladder exstrophy, Breast cancer, Corneal astigmatism, Desbuquois syndrome, Diverticular disease, Liver cirrhosis, Pelvic organ prolapse, Schizophrenia, Vitiligo
12474	54498	SMOX	Spermine oxidase	C20orf16, PAO, PAO-1, PAO1, PAOH, PAOH1, SMO	Alzheimer disease, Androgenetic alopecia, Cerebrovascular disorder, Color vision deficiency, Dementia, Mood disorder, Panic disorder, Stroke, Tooth disease
12475	6609	SMPD1	Sphingomyelin phosphodiesterase 1	ASM, ASMASE, NPD	Acid sphingomyelinase deficiency, Asthma, Neuronal ceroid lipofuscinosis, Visceral acid sphingomyelinase deficiency, Gaucher disease, Insomnia, Intellectual developmental disorder, Kidney disease, Niemann-pick disease, Willis-ekbom disease, Smooth surface dental caries
12476	55512	SMPD3	Sphingomyelin phosphodiesterase 3	NSMASE2	Obstructive pulmonary disease, Leukemia, Metabolic syndrome, Myelodysplastic syndrome, Ovarian cancer, Schizophrenia, Diabetes mellitus type 2
12477	55627	SMPD4	Sphingomyelin phosphodiesterase 4	NEDMABA, NEDMEBA, NET13, NSMASE-3, NSMASE3, SKNY	Neurodevelopmental disorder
12478	10924	SMPDL3A	Sphingomyelin phosphodiesterase acid like 3A	ASM3A, ASML3a, yR36GH4.1	Endometriosis, Sensory peripheral neuropathy
12479	27293	SMPDL3B	Sphingomyelin phosphodiesterase acid like 3B	ASML3B	Corneal astigmatism, Moyamoya disease
12480	23676	SMPX	Small muscle protein X-linked	Chisel, Csl, DFN6, DFNX4, MPD7	Deafness, x-linked, Hearing impairment, Hereditary hearing loss, X-linked nonsyndromic hearing loss

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