All individuals with variants in gene SRD5A3

10 entries on 1 page. Showing entries 1 - 10.
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00209007 28771251-Pat10 PubMed: Lionel 2018 - F - Canada - - - - - ? Complex neurological phenotype 1 1 Johan den Dunnen
00269905 - - - ? - - - - - - - ? Global developmental delay (HP:0001263); Microcephaly (HP:0000252); Seizures (HP:0001250); Muscular hypotonia (HP:0001252); Inability to walk (HP:0002540); Dysphagia (HP:0002015); Developmental glaucoma (HP:0001087) 1 1 IMGAG
00288324 - - - M - - - - - - - ? Cleft palate (HP:0000175); Long philtrum (HP:0000343); Micrognathia (HP:0000347); Hypoplasia of the thymus (HP:0000778); Insulin resistance (HP:0000855); Intrauterine growth retardation (HP:0001511); Enlarged cisterna magna (HP:0002280); Arthrogryposis multiplex congenita (HP:0002804); Hyperglycemia (HP:0003074); Ichthyosis (HP:0008064); Transient neonatal diabetes mellitus (HP:0008255); Camptodactyly (HP:0012385) 1 1 IMGAG
00293632 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00317998 PKMR115 PubMed: Riazuddin 2017 - - yes Pakistan - - - - - ID Not available 1 1 Johan den Dunnen
00382153 59 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - CDG1Q Oculocutaneous albinism and others; MIM, 612379 or 612713 1 1 LOVD
00382154 60 PubMed: Patel 2019 - ? - United Kingdom (Great Britain) - - - - - CDG1Q Oculocutaneous albinism and others; MIM, 612379 or 612713 1 1 LOVD
00383460 - PubMed: Khan 2019 - F - - - - - - - retinal disease - 1 1 LOVD
00403882 TF105 PubMed: Froukh 2020 analysis 103 families with neurodevelopmental disorders - - Jordan - - - - - NDD - 1 1 Johan den Dunnen
00428231 Fam11PatII1 PubMed: Falb 2023, Journal: Falb 2023 family, 1 affected M - Germany - - - - - ? reduced fetal movements, intrauterine growth restriction, human tail, hypertrichosis; contractures elbows, wrists, fingers, hips, knees; micrognathia and retrognathia, dysplastic low-set ears, thin upper lip, sacral human tail, cleft palate, camptodactyly; muscular hypertonia, wide cisterna magna, pathological oculomotor function and otoacoustic emissions; respiratory insufficiency, non-invasive ventilation, laryngomalacia, retinal coloboma, myocardial hypertrophy, myocardial infarction, thymic hypoplasia, hyperglycaemia, insulin resistance, ichthyosis, cryptorchidism 1 1 Johan den Dunnen
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