All individuals with variants in gene SLC35A2

41 entries on 1 page. Showing entries 1 - 41.
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00000208 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), no prolactin deficiency, age sonographic determination testicular volume 17.64y, testicular volume right/left 21/20 (7.3–16ml) 2 1 Yu Sun
00000209 - PubMed: Sun 2011, Journal: Sun 2011 - M no Netherlands - - - - - CHTE central hypothyroidism (FT4 0.50-0.99of lower limit normal), prolactin deficiency, age sonographic determination testicular volume 21.36y, testicular volume right/left 30/26 (8.5–18.3ml) 2 1 Yu Sun
00002413 - - early-onset epileptic encephalopathy F no Japan - - - - - ID early-onset epileptic encephalopathy 1 1 Hirotomo Saitsu
00002414 - - - F no Japan - - - - - ID early-onset epileptic encephalopathy 1 1 Hirotomo Saitsu
00002415 - - early-onset epileptic encephalopathy F no Japan - - - - - ID early-onset West syndrome 1 1 Hirotomo Saitsu
00039394 - PubMed: Bosch 2016, Journal: Bosch 2016 - F no Netherlands - - - - - CVI, ID - 1 1 Danielle Bosch
00207893 28771251-Pat86 PubMed: Lionel 2018 - F - Canada - - - - - ? Global developmental delay; seizures; CNS hypomyelination 1 1 Johan den Dunnen
00208560 - - - F - - - - - - - CDG - 1 1 Bobby Ng
00208561 - - - F no - - - - - - CDG - 1 1 Bobby Ng
00208562 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208564 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208565 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208566 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208568 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208569 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208570 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208571 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208572 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208573 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208574 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208575 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208576 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208577 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208578 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208579 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208580 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208581 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208582 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208583 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208584 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208585 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208586 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208587 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208588 - - - M no - - - - - - CDG2M - 1 1 Bobby Ng
00208589 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208590 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00208591 - - - F no - - - - - - CDG2M - 1 1 Bobby Ng
00288200 Pat10 PubMed: Lee 2019 - - - United States - - - - - ? microcephaly, failure to thrive, hemihypertrophy of lower limb, strabismus, cortical visual impairment, hypermetropia, central sleep apnea, muscular hypotonia, reduced intestinal motility, global developmental delay, decreased CSF homovanillic acid, infantile spasms, hypsarrhythmia, cerebellar vermis atrophy, cerebral white matter atrophy, osteopenia, decreased serum creatinine, increased IgM level, erythrocyte macrocytosis, low alkaline phosphatase, hypoalbuminemia, abnormal lymphocyte count, monocytosis, increased serum testosterone level, premature adrenarche, neutropenia, hypoglycemia, abnormal neutrophil cell number 1 1 Johan den Dunnen
00324421 CFD4A PubMed: Cao 2020 2-generation family, 1 affected, unaffected heterozygous carrier parents - - - - - - - - ? - 1 1 Johan den Dunnen
00387699 M002 PubMed: Hu 2019 family, 2 affected individuals, third cousin parents - yes Iran Persia - - - - ID syndromic intellectual disability, no microcephaly 1 2 Johan den Dunnen
00448210 Pat90 PubMed: Poli 2024 - F - Chile - - - - - ? developmental delay; retinitis pigmentosa; hypotonia; hypoplasia of the corpus callosum; short stature; immune system dysfunction (sepsis) 1 1 Johan den Dunnen
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