Disease #05148 (SINO (SINO syndrome (spastic paraplegia, intellectual disability, nystagmus, and obesity)))

Official abbreviation SINO
Name SINO syndrome (spastic paraplegia, intellectual disability, nystagmus, and obesity)
OMIM ID -
Inheritance -
Individuals reported having this disease 3
Phenotype entries for this disease 3
Associated with 1 gene KIDINS220
Associated tissues -
Disease features -
Remarks -
Date created 2016-04-01 10:04:21 +02:00 (CEST)
Date last edited N/A


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00060315 - PubMed: Josifova 2016, Journal: Josifova 2016 - M no Netherlands - - - - - SINO spastic paraplegia (HP:0001258), intellectual disability (HP:0001249), nystagmus (HP:0000639), obesity (HP:0001513) - KIDINS220 1 1 Glen Monroe
00060316 - PubMed: Josifova 2016, Journal: Josifova 2016 - M no Netherlands - - - - - SINO spastic paraplegia (HP:0001258), intellectual disability (HP:0001249), nystagmus (HP:0000639), obesity (HP:0001513) - KIDINS220 1 1 Glen Monroe
00060317 - PubMed: Josifova 2016, Journal: Josifova 2016 - M no United Kingdom (Great Britain) - - - - - SINO spastic paraplegia (HP:0001258), intellectual disability (HP:0001249), nystagmus (HP:0000639), obesity (HP:0001513) - KIDINS220 1 1 Glen Monroe
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