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Disease	Synonyms	Description	Articles
syndromic X-linked intellectual disability Raymond type	mental retardation, X-linked syndromic, Raymond ty.. [+] mental retardation, X-linked syndromic, Raymond type; MRXSR; X-linked syndromic intellectual developmental disorder Raymond type [-]	A syndromic X-linked intellectual disability chara..[+] A syndromic X-linked intellectual disability characterized by intellectual disability and marfanoid habitus that has_material_basis_in mutation in the ZDHHC9 gene on chromosome Xq26.1. [-]
syndromic X-linked intellectual disability Shashi type	Shashi X-linked mental retardation syndrome; syndr.. [+] Shashi X-linked mental retardation syndrome; syndromic X-linked intellectual disability type 11; SMRXS; mental retardation, X-linked, syndromic 11, Shashi type; MRXS11; X-linked mental retardation Shashi type [-]	A syndromic X-linked intellectual disability chara..[+] A syndromic X-linked intellectual disability characterized by moderate intellectual deficit, obesity, macroorchidism and a characteristic facies that has_material_basis_in mutation in the RBMX gene on chromosome Xq26. [-]
septooptic dysplasia	septo-optic dysplasia; SOD; De Morsier syndrome	A syndrome characterized by the classical triad of..[+] A syndrome characterized by the classical triad of optic nerve hypoplasia, pituitary gland hypoplasia and midline brain defects that has_material_basis_in mutation in the HESX1 gene on chromosome 3p14. [-]
salmonellosis	Salmonella infection	A primary bacterial infectious disease caused by t..[+] A primary bacterial infectious disease caused by the bacteria of the genus Salmonella. It has symptoms diarrhea, fever, vomiting, and abdominal cramps 12 to 72 hours after infection. In most cases, the illness lasts four to seven days, and most people recover without treatment. [-]
Seckel syndrome 9	SCKL9	A Seckel syndrome that has_material_basis_in homoz..[+] A Seckel syndrome that has_material_basis_in homozygous mutation in the TRAIP gene on chromosome 3p21. [-]
Seckel syndrome 6	SCKL6	A Seckel syndrome that has_material_basis_in homoz..[+] A Seckel syndrome that has_material_basis_in homozygous mutation in the CEP63 gene on chromosome 3q22. [-]
Seckel syndrome 1	SCKL1; microcephalic primordial dwarfism I	A Seckel syndrome that has_material_basis_in homoz..[+] A Seckel syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the ATR gene on chromosome 3q23. [-]	1 articles
Seckel syndrome 10	SCKL10	A Seckel syndrome that has_material_basis_in compo..[+] A Seckel syndrome that has_material_basis_in compound heterozygous mutation in the NSMCE2 gene on chromosome 8q24. [-]
Seckel syndrome 8	SCKL8	A Seckel syndrome that has_material_basis_in homoz..[+] A Seckel syndrome that has_material_basis_in homozygous mutation in the DNA2 gene on chromosome 10q21. [-]
Seckel syndrome 4	SCKL4	A Seckel syndrome that has_material_basis_in homoz..[+] A Seckel syndrome that has_material_basis_in homozygous mutation in the CENPJ gene on chromosome 13q12. [-]
Seckel syndrome 7	SCKL7	A Seckel syndrome that has_material_basis_in compo..[+] A Seckel syndrome that has_material_basis_in compound heterozygous mutation in the NIN gene on chromosome 14q22. [-]
Seckel syndrome 5	SCKL5	A Seckel syndrome that has_material_basis_in homoz..[+] A Seckel syndrome that has_material_basis_in homozygous or compound heterozygous mutation in the CEP152 gene on chromosome 15q21. [-]
Seckel syndrome 2	SCKL2; Seckel-type dwarfism 2; microcephalic primo.. [+] Seckel-type dwarfism 2; SCKL2; microcephalic primordial dwarfism 2 [-]	A Seckel syndrome that has_material_basis_in homoz..[+] A Seckel syndrome that has_material_basis_in homozygous mutation in the RBBP8 gene on chromosome 18q11. [-]	1 articles
Schuurs-Hoeijmakers Syndrome	SHMS; autosomal dominant mental retardation 17; MR.. [+] SHMS; autosomal dominant mental retardation 17; MRD17 [-]	An autosomal dominant intellectual developmental d..[+] An autosomal dominant intellectual developmental disorder that has_material_basis_in an autosomal dominant mutation of the PACS1 gene on chromosome 11q13.1-q13.2. [-]
schizophrenia 1	SCZD1	A schizophrenia that has_material_basis_in an auto..[+] A schizophrenia that has_material_basis_in an autosomal dominant mutation of the SCZD1 gene on chromosome 5q23-q35. [-]
schizophrenia 2	SCZD2	A schizophrenia that has_material_basis_in an auto..[+] A schizophrenia that has_material_basis_in an autosomal dominant mutation of the SCZD2 gene on chromosome 11q14-q21. [-]
schizophrenia 3	SCZD3	A schizophrenia that has_material_basis_in an auto..[+] A schizophrenia that has_material_basis_in an autosomal dominant mutation of the SCZD3 gene on chromosome 6p23. [-]
schizophrenia 4	SCZD4	A schizophrenia that has_material_basis_in an auto..[+] A schizophrenia that has_material_basis_in an autosomal dominant mutation of the PRODH gene on chromosome 22q11.21. [-]
schizophrenia 5	SCZD5	A schizophrenia that has_material_basis_in a mutat..[+] A schizophrenia that has_material_basis_in a mutation on chromosome 6q13-q26. [-]
schizophrenia 6	SCZD6	A schizophrenia that has_material_basis_in an auto..[+] A schizophrenia that has_material_basis_in an autosomal dominant mutation of the SCZD6 gene on chromosome 8p21. [-]
schizophrenia 7	SCZD7	A schizophrenia that has_material_basis_in an auto..[+] A schizophrenia that has_material_basis_in an autosomal dominant mutation of the SCZD7 gene on chromosome 13q32. [-]
schizophrenia 8	SCZD8	A schizophrenia that has_material_basis_in an auto..[+] A schizophrenia that has_material_basis_in an autosomal dominant mutation of the SCZD8 gene on chromosome 18p. [-]
schizophrenia 9	SCZD9	A schizophrenia that has_material_basis_in a mutat..[+] A schizophrenia that has_material_basis_in a mutation of the DISC1 gene on chromosome 1q42.2. [-]
schizophrenia 10	SCZD10	A schizophrenia that has_material_basis_in an auto..[+] A schizophrenia that has_material_basis_in an autosomal dominant mutation of the SCZD10 gene on chromosome 15q15. [-]
schizophrenia 11	SCZD11	A schizophrenia that has_material_basis_in a mutat..[+] A schizophrenia that has_material_basis_in a mutation on chromosome 10q22.3. [-]
schizophrenia 12	SCZD12	A schizophrenia that has_material_basis_in a mutat..[+] A schizophrenia that has_material_basis_in a mutation on chromosome 1p36.2. [-]
schizophrenia 13	SCZD13	A schizophrenia that has_material_basis_in a mutat..[+] A schizophrenia that has_material_basis_in a mutation on chromosome 15q13. [-]
schizophrenia 14	SCZD14	A schizophrenia that has_material_basis_in a mutat..[+] A schizophrenia that has_material_basis_in a mutation on chromosome 2q32.1. [-]
schizophrenia 15	SCZD15	A schizophrenia that has_material_basis_in a mutat..[+] A schizophrenia that has_material_basis_in a mutation of the SHANK3 gene on chromosome 22q13.33. [-]
schizophrenia 16	SCZD16	A schizophrenia that has_material_basis_in a mutat..[+] A schizophrenia that has_material_basis_in a mutation on chromosome 7q36.3. [-]
schizophrenia 18	SCZD18; Chromosome 7q36.3 Duplication Syndrome, 36.. [+] SCZD18; Chromosome 7q36.3 Duplication Syndrome, 362-Kb [-]	A schizophrenia that has_material_basis_in a mutat..[+] A schizophrenia that has_material_basis_in a mutation of the SLC1A1 gene on chromosome 9p24.2. [-]
spermatogenic failure 21		A male infertility characterized by acephalic sper..[+] A male infertility characterized by acephalic spermatozoa, reduced sperm number and impaired sperm motility that has_material_basis_in homozygous mutation in the BRDT gene on chromosome 1p22. [-]
spermatogenic failure 2	SPGF2	A spermatogenic failure that is characterized by a..[+] A spermatogenic failure that is characterized by azoospermia or severe oligozoospermia that has_material_basis_in inversions on chromosome 1. [-]
spermatogenic failure 18	SPGF18	A spermatogenic failure that is characterized by s..[+] A spermatogenic failure that is characterized by sperm flagellar morphological abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the DNAH1 gene on chromosome 3p21. [-]
spermatogenic failure 20	SPGF20	A spermatogenic failure that is characterized by a..[+] A spermatogenic failure that is characterized by autosomal recessive inheritance of sperm flagellar morphological abnormalities that has_material_basis_in mutation in the CFAP44 gene on chromosome 3q13. [-]
spermatogenic failure 6	SPGF6	A male infertility characterized by autosomal rece..[+] A male infertility characterized by autosomal recessive inheritance of globozoospermia that has_material_basis_in mutation in the SPATA16 gene on chromosome 3q26. [-]
spermatogenic failure 3	SPGF3	A spermatogenic failure that is characterized by a..[+] A spermatogenic failure that is characterized by autosomal dominant inheritance of nonobstructive asthenozoospermia that has_material_basis_in heterozygous mutation in the SLC26A8 gene on chromosome 6p21. [-]
spermatogenic failure 8	SPGF8	A spermatogenic failure that is characterized by a..[+] A spermatogenic failure that is characterized by autosomal dominant inheritance of azoospermia or moderate to severe oligozoospermia that has_material_basis_in heterozygous mutation in the NR5A1 gene on chromosome 9q33. [-]
spermatogenic failure 19	SPGF19	A spermatogenic failure that is characterized by a..[+] A spermatogenic failure that is characterized by autosomal recessive inheritance of sperm flagellar morphological abnormalities that has_material_basis_in mutation in the CFAP43 gene on chromosome 10q25. [-]
spermatogenic failure 12	SPGF12	A spermatogenic failure that is characterized by a..[+] A spermatogenic failure that is characterized by autosomal dominant inheritance of azoospermia or severe oligoasthenoteratozoospermia and in some cases a Sertolic cell-only phenotype that has_material_basis_in heterozygous mutation in the NANOS1 gene on chromosome 10q26. [-]
spermatogenic failure 15	SPGF15	A spermatogenic failure that is characterized by a..[+] A spermatogenic failure that is characterized by autosomal recessive inheritance of azoospermia that has_material_basis_in mutation in the SYCE1 gene on chromosome 10q26. [-]
spermatogenic failure 7	SPGF7	A spermatogenic failure that is characterized by a..[+] A spermatogenic failure that is characterized by autosomal recessive inheritance of impaired or absent sperm motility and increased incidence of morphologically abnormal sperm that has_material_basis_in mutation in the CATSPER1 gene on chromosome 11q13. [-]
spermatogenic failure 17	SPGF17; Male infertility due to oocyte activation .. [+] SPGF17; Male infertility due to oocyte activation failure [-]	A spermatogenic failure that is characterized by a..[+] A spermatogenic failure that is characterized by autosomal recessive inheritance of oocyte activation failure following intracytoplasmic sperm injection that has_material_basis_in mutation in the PLCZ1 gene on chromosome 12p12. [-]
spermatogenic failure 4	SPGF4	A spermatogenic failure that is characterized by a..[+] A spermatogenic failure that is characterized by autosomal dominant inheritance of nonobstructive azoospermia caused by meiotic abnormalities that has_material_basis_in mutation in the SYCP3 gene on chromosome 12q23. [-]
spermatogenic failure 22	SPGF22	A spermatogenic failure that is characterized by a..[+] A spermatogenic failure that is characterized by autosomal recessive inheritance of spermatocyte maturation arrest resulting in azoospermia that has_material_basis_in mutation in the MEIOB gene on chromosome 16p13. [-]
spermatogenic failure 10	Spermatogenic failure with defective sperm annulus.. [+] Spermatogenic failure with defective sperm annulus; SPGF10 [-]	A spermatogenic failure that is characterized by d..[+] A spermatogenic failure that is characterized by defects in the annulus or the ring-like structure located at the distal end of the flagellar midpiece the autosomal dominant inheritance of that has_material_basis_in mutation in the SEPT12 gene on chromosome 16p13. [-]
spermatogenic failure 14	SPGF14	A spermatogenic failure that is characterized by a..[+] A spermatogenic failure that is characterized by autosomal recessive inheritance of a maturation arrest in the spermatid stage of development that has_material_basis_in mutation in the ZMYND15 gene on chromosome 17p13. [-]
spermatogenic failure 11	SPGF11	A spermatogenic failure that is characterized by a..[+] A spermatogenic failure that is characterized by autosomal dominant inheritance of oligozoospermia and in some cases teratozoospermia and/or moderate asthenozoospermia that has_material_basis_in mutation in the KLHL10 gene on chromosome 17q21. [-]
spermatogenic failure 23	SPGF23	A spermatogenic failure that is characterized by a..[+] A spermatogenic failure that is characterized by autosomal recessive inhertitance of nonobstructive azoospermia that has_material_basis_in mutation in the TEX14 gene on chromosome 17q23. [-]
spermatogenic failure 13	SPGF13	A spermatogenic failure that is characterized by a..[+] A spermatogenic failure that is characterized by autosomal recessive inheritance of azoospermia or oligozoospermia that has_material_basis_in mutation in the TAF4B gene on chromosome 18q11. [-]

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