All individuals with variants in gene ZMYM3

34 entries on 1 page. Showing entries 1 - 34.
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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) 1 1 Yu Sun
00173387 19377476-Pat? PubMed: Tarpey 2009 - M - - - - - for details contact Lucy Raymond (flr24 @ cam.ac.uk) - MRX;IDX - 1 2 Lucy Raymond
00173388 19377476-Pat? PubMed: Tarpey 2009 - M - - - - - for details contact Lucy Raymond (flr24 @ cam.ac.uk) - MRX;IDX - 1 1 Lucy Raymond
00311162 B1287-21 PubMed: Connaughton 2020 - M - - - - - - - CAKUT see paper; ... 1 1 Johan den Dunnen
00311163 B2323-21 PubMed: Connaughton 2020 - M - - - - - - - CAKUT see paper; ... 1 1 Johan den Dunnen
00399156 FamD222 PubMed: Philips 2014 3-generation family, 3 affected (3M), unaffected heterozygous carrier mother M - Finland - - - - - ID see paper; ... 1 3 Johan den Dunnen
00418697 Fam1 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, unaffected carrier mother M - - - - - - - NDD speech delay; motor delay; no behavioral problems; no facial dysmorphism; urinary tract dilatation of left kidney on ultrasound; congenital heart defects 1 1 Johan den Dunnen
00418698 Fam2 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, carrier mother history of learning disability M - - - - - - - NDD speech delay; motor delay; no intellectual disability; no autism spectrum disorder; no behavioral problems; facial dysmorphism; no genitourinary anomalies; history of growth hormone resistance and IGF1 deficiency (basis unknown), fasting and heat intolerance, excessive fatigue 1 1 Johan den Dunnen
00418699 Fam3 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, unaffected carrier mother M - - - - - - - NDD speech delay; motor delay; autism spectrum disorder; behavioral problems; facial dysmorphism; pielonephritis, vesicoureteral reflux; gastroesophageal reflux disease 1 1 Johan den Dunnen
00418700 Fam4PatA Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 2 affected brothers, unaffected carrier mother M - - - - - - - NDD speech delay; motor delay; intellectual disability; autism spectrum disorder; behavioral problems; facial dysmorphism; hypospadias 1 2 Johan den Dunnen
00418701 Fam4PatB Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 brother M - - - - - - - NDD speech delay; no motor delay; intellectual disability; autism spectrum disorder; behavioral problems; facial dysmorphism; no genitourinary anomalies 1 1 Johan den Dunnen
00418702 Fam5 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, unaffected carrier mother M - - - - - - - NDD speech delay; motor delay; intellectual disability; autism spectrum disorder; behavioral problems; no facial dysmorphism; no genitourinary anomalies; weight <1%ile 1 1 Johan den Dunnen
00418703 Fam6 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, carrier mother attention deficit-hyperactivity disorder M - - - - - - - NDD speech delay; motor delay; intellectual disability; autism spectrum disorder; behavioral problems; facial dysmorphism; single renal cyst; constipation 1 1 Johan den Dunnen
00418704 Fam7 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, unaffected carrier mother M - - - - - - - MPS4A, NDD speech delay; motor delay; intellectual disability; autism spectrum disorder; behavioral problems; facial dysmorphism; cryptorchidism, enuresis; short stature; mild features MPS4A (skeletal phenotype) caused by GALNS variants 1 1 Johan den Dunnen
00418705 Fam8 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, carrier mother history of learning disability M - - - - - - - NDD speech delay; motor delay; intellectual disability; autism spectrum disorder; behavioral problems; facial dysmorphism; hypospadias, ambiguous genitalia; short stature 1 1 Johan den Dunnen
00418706 Fam9PatA Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 2 affected brothers, unaffected carrier mother M yes - - - - - - NDD speech delay; no motor delay; intellectual disability; autism spectrum disorder; behavioral problems; facial dysmorphism; no genitourinary anomalies 1 2 Johan den Dunnen
00418707 Fam9PatB Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 brother M yes - - - - - - NDD speech delay; no motor delay; intellectual disability; autism spectrum disorder; behavioral problems; facial dysmorphism; no genitourinary anomalies 1 1 Johan den Dunnen
00418708 Fam10 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, carrier mother history of dyslexia M - - - - - - - NDD speech delay; no motor delay; behavioral problems; facial dysmorphism; no genitourinary anomalies; gastroesophageal reflux disease, constipation 1 1 Johan den Dunnen
00418709 Fam11 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, unaffected carrier mother M - - - - - - - NDD speech delay; no motor delay; intellectual disability; no autism spectrum disorder; behavioral problems; facial dysmorphism; ectopic kidney; short stature, kyphoscoliosis 1 1 Johan den Dunnen
00418710 Fam12 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, unaffected carrier mother M - - - - - - - NDD speech delay; motor delay; intellectual disability; no autism spectrum disorder; behavioral problems; facial dysmorphism; no genitourinary anomalies; microcephaly 1 1 Johan den Dunnen
00418711 Fam13 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, unaffected non carrier parents M - - - - - - - NDD speech delay; motor delay; intellectual disability; no autism spectrum disorder; behavioral problems; facial dysmorphism; cryptorchidism; microcephaly, short stature, weight <3%ile, kyphosis, long bone defects, Madelung deformity; 1 1 Johan den Dunnen
00418712 Fam14 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, unaffected parents M - - - - - - - NDD speech delay; motor delay; intellectual disability; no autism spectrum disorder; no behavioral problems; no facial dysmorphism; enuresis; microcephaly, scoliosis, reflux 1 1 Johan den Dunnen
00418713 Fam15 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, unaffected non carrier parents M - - - - - - - NDD speech delay; motor delay; intellectual disability; autism spectrum disorder; behavioral problems; facial dysmorphism; no genitourinary anomalies; microcephaly, scoliosis 1 1 Johan den Dunnen
00418714 Fam16 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, unaffected non carrier parents M - - - - - - - NDD deceased 1 1 Johan den Dunnen
00418715 Fam17 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, unaffected carrier mother M - - - - - - - NDD speech delay; motor delay; no intellectual disability; autism spectrum disorder; behavioral problems; no facial dysmorphism; no genitourinary anomalies; GI dysmotility, joint laxity, pain and swelling, dysautonomic symptoms 1 1 Johan den Dunnen
00418716 Fam18 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, unaffected carrier mother F - - - - - - - NDD speech delay; motor delay; no behavioral problems; facial dysmorphism; no genitourinary anomalies; gastroesophageal reflux disease 1 1 Johan den Dunnen
00418717 Fam19 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, unaffected non carrier parents F - - - - - - - NDD speech delay; motor delay; no behavioral problems; facial dysmorphism; no genitourinary anomalies 1 1 Johan den Dunnen
00418718 Fam20 Journal: Hiatt 2022, PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, unaffected non carrier parents F - - - - - - - NDD speech delay; motor delay; facial dysmorphism; pyelectasis; volvulus of midgut, pancreatic cysts 1 1 Johan den Dunnen
00428767 Pat21 PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, unaffected parents M - - - - - - - NDD see paper; ..., speech delay, no motor delay, intellectual disability, autistic traits, behavioral problems, dysmorphism, hypospadias 1 1 Johan den Dunnen
00428768 Pat22 PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 2 affected (sister/brother), unaffected parents M - - - - - - - NDD see paper; ..., speech delay, no motor delay, intellectual disability, autistic traits, no behavioral problems, dysmorphism, no genitourinary anomalies; mild short stature 1 2 Johan den Dunnen
00428769 Pat23 PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, unaffected heterozygous carrier parents M - - - - - - - NDD see paper; ..., speech delay, motor delay, no intellectual disability, no autistic traits, behavioral problems, dysmorphism, genitourinary anomalies (vesicoureteral reflux); short stature, microcephaly, myopia, retinopathy, GI dysmotility 1 1 Johan den Dunnen
00428770 Pat24 PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 2 affected, boy and affected carrier mother M - - - - - - - NDD see paper; ..., speech delay, motor delay, intellectual disability, autistic traits, no behavioral problems, dysmorphism, no genitourinary anomalies; mother ADHD, history of delays 1 2 Johan den Dunnen
00428771 Pat25 PubMed: Hiatt 2023, Journal: Hiatt 2023 2-generation family, 1 affected, unaffected carrier mother M - - - - - - - NDD see paper; ..., speech delay, no motor delay, intellectual disability, autistic traits, behavioral problems, no dysmorphism, no genitourinary anomalies 1 1 Johan den Dunnen
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