All individuals with variants in gene ASPH

3 entries on 1 page. Showing entries 1 - 3.
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00375522 - - - F - - - - - - - ? Inguinal hernia (HP:0000023); Ectopia lentis (HP:0001083); Meningocele (HP:0002435); Scoliosis (HP:0002650); Abnormality of connective tissue (HP:0003549); Vitreous hemorrhage (HP:0007902); Clinodactyly (HP:0030084); Arachnoid cyst (HP:0100702); Dural ectasia (HP:0100775) 1 1 IMGAG
00451694 ASPH-01 PubMed: Chen 2024, Journal: Chen 2024 2-generation family, 1 affected, unaffected heterozygous parents M yes China Chinese - - - - Traboulsi Facial dysmorphic features were remarkable including long appearance, retrognathia, malar hypoplasia, and dental malocclusion.The lens was subluxated anteriorly with a shallow anterior chamber bilaterally. As is quantified by AS-OCT, the lens had reduced equatorial d 1 1 Wannan Jia
00451695 ASPH-02 PubMed: Chen 2024, Journal: Chen 2024 2-generation family, 1 affected, unaffected heterozygous parents M no China Chinese - - - - Traboulsi Facial dysmorphic features were remarkable including long appearance, retrognathia, and malar hypoplasia. Anteriorly dislocated micropherophakic lenses were observed. 2 1 Wannan Jia
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