All individuals with variants in gene MAN1B1

9 entries on 1 page. Showing entries 1 - 9.
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Owner     
00016306 - - family, 2 affected brothers M yes Palestine Palestinian - - - - ID cranio-lenticulo-sutural dysplasia (CLSD) and congenital disorders of glycosylation (CDG)-II 1 2 Swati Gupta
00248406 - - - M - - - - - - - - HP:0012759 (Neurodevelopmental abnormality); HP:0012373 (Abnormal eye physiology); HP:0001263 (Global developmental delay); HP:0000284 (Abnormality of the ocular region); HP:0010621 (Cutaneous syndactyly of toes); HP:0003011 (Abnormality of the musculature); HP:0000316 (Hypertelorism); HP:0000508 (Ptosis); HP:0005709 (2-3 toe cutaneous syndactyly); HP:0000301 (Abnormality of facial musculature) 1 1 Andreas Laner
00294814 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 78 Mohammed Faruq
00294815 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 4 Mohammed Faruq
00294816 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 1 Mohammed Faruq
00295327 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 3 Mohammed Faruq
00303626 Family_36 PubMed: Makrythanasis 2014 family, 2 affected - yes Egypt - - - - - ? see paper; ..., syndromic intellectual disability/developmental delay 1 2 Johan den Dunnen
00305239 - PubMed: Narang 2020, Journal: Narang 2020 analysis 2794 individuals (India) - - India - - - - - ? - 1 2 Mohammed Faruq
00327001 174406 - - F - - Arabia - - - - MRT15 (+) Neurodevelopmental delay, brother aslo affected 1 1 Andreas Laner
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