Phenotypes for disease #00907 (MSS (Marinesco-Sjogren syndrome (MSS)), OMIM:248800)

3 entries on 1 page. Showing entries 1 - 3.
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AscendingPhenotype ID     

Phenotype details     

Diagnosis/Initial     

Diagnosis/Definite     

Inheritance     

Age/Examination     

Age/Diagnosis     

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Individual ID     
0000334603 see paper; ..., cataracts, ataxia, delayed growth, mental retardation chylomicron retention disease - Marinesco-Sjogren syndrome MSS Familial, autosomal recessive - - - - - Johan den Dunnen 00445351
0000334604 see paper; ..., cataracts, ataxia, delayed growth, mental retardation chylomicron retention disease - Marinesco-Sjogren syndrome MSS Familial, autosomal recessive - - - - - Johan den Dunnen 00445352
0000357497 see paper; ..., congenital hypotonia; delayed motor development, 1y6m-head control, 2y-sit, 15y-walk supported; no intellectual disability; 20m-MRI cranial diffuse cerebellar vermian atrophic volume loss, cortical-dominant degenerative T2 FLAIR hyperintensity changes infratentorial level; strabismus, cataract; microcephaly congenital hypotonia MSS Familial, autosomal recessive 15y - - - - Johan den Dunnen 00472700
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