All individuals with variants in gene OCRL

21 entries on 1 page. Showing entries 1 - 21.
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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) 3 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) 3 1 Yu Sun
00050662 - PubMed: DDDS 2015, Journal: DDDS 2015 family, 1 affected M - United Kingdom (Great Britain) - - - Decipher - ? global developmental delay, delayed speech and language development, feeding difficulties in infancy, cryptorchidism, plagiocephaly, pectus carinatum, abnormal facial shape, deeply set eye, high anterior hairline, broad forehead, macrotia, clinodactyly of the 5th finger, abnormality of the palmar creases, skin dimples, intrauterine growth retardation, short stature, delayed gross motor development, joint hypermobility 1 1 Johan den Dunnen
00174395 - - - ? - (Germany) - - - - - ? HP:0001252 (Muscular hypotonia) 1 1 IMGAG
00235341 - - - M - - - - - - - ? Seizures (HP:0001250); Cataract (HP:0000518) 1 1 IMGAG
00246689 00004 - - - - - - - - - - OCRL - 1 1 Xia Zhang
00307959 15DG0115 PubMed: Anazi 2017 simplex case M - - - - - - - ID see paper; ..., Congenital cataract, Nephrocalcinosis, Global developmental delay, Sparse hair, Fair hair, Microphthalmia, Hypotonia, Hyperreflexia 1 1 Johan den Dunnen
00374429 S-3192 PubMed: Ganapathy 2019 - - - India - - - - - ? Global developmental delay, congenital cataract, hypotonia, umbilical hernia, failure to thrive, vitamin D deficiency and seizures 1 1 Johan den Dunnen
00374792 S-1274 PubMed: Ganapathy 2019 - - - India - - - - - ? - 1 1 Johan den Dunnen
00403763 patient PubMed: Rendu 2017 2-generation family, 1 affected, unaffected heterozygous carrier mother - - France - - - - - OCRL born at term; normal motor milestones; delayed speech and language; 3y-short stature, bilateral cataracts ; 5y-acute and chronic renal failure after 3w episode of vomiting, headaches, weight loss 1 1 Johan den Dunnen
00414363 WHP30 PubMed: Sun 2018 - M - China - - - - - ? Dent Disease 2; Cystinuria 1 1 LOVD
00414394 WHP61 PubMed: Sun 2018 - M - China - - - - - ? - 1 1 LOVD
00414441 WHP108 PubMed: Sun 2018 - M - China - - - - - ? Primary Hyperoxaluria Type 1;Dent Disease 2 1 1 LOVD
00444921 Fam38PatII2 PubMed: Ma 2016 3-generation family, affected mother/son/daughter F - Australia - - - - - CTRCT see paper; ..., bilateral cataract, aphakic glaucoma, buphthalmos, scleromalacia; mother cataracts, brother cataracts, nonverbal/intellectual disability 1 3 Johan den Dunnen
00445050 CCMR00491 PubMed: Kessel 2021 patient - - Denmark - - - - - CTRCT bilateral cataract, Lowe syndrome 1 1 Johan den Dunnen
00464361 - - - - - - - - - - - DENT2 - 1 1 Min Peng
00466836 Pat123 PubMed: Tuysuz 2022 - - - Turkey - - - - - OI - 1 1 Johan den Dunnen
00468503 Pat62 PubMed: Wang 2024 patient, no family history M - China - - - - - CTRCT thin cataract, fibrotic nuclear cataract; symmetrical opacities; muscular hypotonia, nystagmus, tooth defects, kidney defect, cognitive impairment 1 1 Johan den Dunnen
00468504 Pat63 PubMed: Wang 2024 family M - China - - - - - CTRCT thin cataract, fibrotic nuclear cataract; symmetrical opacities; decreased height, muscular defects 1 2 Johan den Dunnen
00468505 Pat64 PubMed: Wang 2024 patient, no family history M - China - - - - - CTRCT thin cataract, fibrotic nuclear cataract; symmetrical opacities; iris heterochromia, muscular hypotonia, nystagmus, tooth defects, kidney defect, cognitive impairment 1 1 Johan den Dunnen
00468506 Pat65 PubMed: Wang 2024 patient, no family history M - China - - - - - CTRCT thin cataract, fibrotic nuclear cataract; symmetrical opacities; muscular hypotonia, nystagmus, glaucoma, tooth defects, kidney defect, cognitive impairment 1 1 Johan den Dunnen
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