Disease #00017 (MRXS10 (mental retardation, X-linked syndromic, type 10 (MRXS-10)), OMIM:300220)

Official abbreviation MRXS10
Name mental retardation, X-linked syndromic, type 10 (MRXS-10)
OMIM ID 300220
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 3
Phenotype entries for this disease 4
Associated with 1 gene HSD17B10
Associated tissues -
Disease features -
Remarks -
Date created 2012-07-23 10:48:25 +02:00 (CEST)
Date last edited 2020-05-11 15:16:08 +02:00 (CEST)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00001698 - PubMed: Reyniers 1999, PubMed: Lenski 2007, Patient IV-1 - M ? Luxembourg - - - - - MRXS10 ascertainment clinical presentation; mild mental retardation, choreoathetosis, abnormal behavior HSD17B10 HSD17B10 1 1 Division of Human Genetics, Innsbruck
00001699 - PubMed: Tarpey 2009 - ? ? - - - - - - MRXS10 ascertainment clinical presentation; mental retardation HSD17B10 HSD17B10 1 1 Division of Human Genetics, Innsbruck
00029716 - - - M - - - - - - - MRXS10 mental retardation, different syndromes HSD17B10 - - 1 Claus Lenski
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