All individuals with variants in gene SMG9

8 entries on 1 page. Showing entries 1 - 8.
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AscendingIndividual ID     

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00065158 27018474Fam1PatIV5 PubMed: Shaheen 2016, Journal: Shaheen 2016 4-generation family, 2 deceased siblings (F, M), unaffected non-carrier parents F yes Saudi Arabia - <00y02m - - - ? Multiple Congenital Anomaly Syndrome: prominent forehead (HP:0011220), Prominent occiput (HP:0000269), low set ears (HP:0000369) malformed ears (HP:0000377), microphthalmia (HP:0000568), depressed nasal bridge (HP:0005280), anteverted nares (HP:0000463), High, narrow palate (HP:0002705), Hand clenching (HP:0001188), Camptodactyly (HP:0012385), Dandy-Walker malformation (HP:0001305), cerebellar vermis hypoplasia (HP:0001320), Hypoplasia of the corpus callosum (HP:0002079), Interrupted aortic arch (HP:0011611), Hypoplastic tricuspid valve (HP:0011573), Hypoplastic aortic arch (HP:0012304), Large muscular ventricular septal defect (HP:0011623) 1 2 Pieter Klap
00065159 27018474-Fam2PatV1 PubMed: Shaheen 2016, Journal: Shaheen 2016 5-generation family, 2 affecteds (2F), unaffected non-carrier parents, Fam2PatV1 F yes Qatar - >03y - - - ? Multiple Congenital Anomaly Syndrome: narrow forehead (HP:0000341), posteriorly rotated ears (HP:0000358), attached ear lobules (HP_:000363), hypertelorism (HP:0000316), Visual impairment (HP:0000505), Wide nasal bridge (HP:0000431), everted lower lip (HP:0000232), Thick lower lip (HP:0000179), right-sided cleft lip (HP:0100333), 2-3 toe syndactyly (HP:0004691), Dandy-Walker malformation (HP:0001305), decreased myelination (HP:0003429), brain atrophy (HP:0012444), large ventricular septal defect (HP:0001629), 1 2 Pieter Klap
00065160 27018474-Fam2PatV3 PubMed: Shaheen 2016, Journal: Shaheen 2016 Fam2PatV3 F yes Qatar - >02y - - - ? Multiple Congenital Anomaly Syndrome: truncal hypotonia (HP:000893), limb hypertonia (HP:0002509), Hyperactive deep tendon reflexes (HP:0006801), adductor spasm in both lower limbs (HP:0002061), ventricular septal defect (HP:0001629) 1 1 Pieter Klap
00234401 - - - F - - - - - - - ? Abnormal facial shape (HP:0001999); Low-set, posteriorly rotated ears (HP:0000368); Long philtrum (HP:0000343); Hypoplasia of the corpus callosum (HP:0002079); Cataract (HP:0000518); Ventricular septal defect (HP:0001629); Failure to thrive (HP:0001508) 1 1 IMGAG
00361514 14DG1661 PubMed: Anazi 2017 familial F yes Saudi Arabia - - - - - ID syndromic; global developmental delay, dysmorphism, microcephaly, congenital heart disease and hypertonia 1 1 Johan den Dunnen
00377062 Fam1 PubMed: Rahikkala 2022, Journal: Rahikkala 2022 - M no Finland - - - - - HBMS - 1 1 Elisa Rahikkala
00377063 Fam2 PubMed: Rahikkala 2022, Journal: Rahikkala 2022 - M no Finland - - - - - HBMS - 1 2 Elisa Rahikkala
00377064 Fam3 PubMed: Rahikkala 2022, Journal: Rahikkala 2022 - M no Finland - - - - - HBMS - 1 2 Elisa Rahikkala
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