Disease #02209 (MRX101 (mental retardation, X-linked, type 101 (MRX101)), OMIM:300928)

Official abbreviation MRX101
Name mental retardation, X-linked, type 101 (MRX101)
OMIM ID 300928
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked recessive
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 1 gene MID2
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Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00114703 19377241-Pat? PubMed: Tarpey 2009 - - - - - - 0 for details contact Lucy Raymond (flr24 @ cam.ac.uk) - MRX101 Intellectual disability; for details please contact Lucy Raymond (flr24 @ cam.ac.uk) MID2 MID2 1 9 Lucy Raymond
00114704 19377242-Pat? PubMed: Tarpey 2009 - - - - - - 0 for details contact Lucy Raymond (flr24 @ cam.ac.uk) - MRX101 Intellectual disability; for details please contact Lucy Raymond (flr24 @ cam.ac.uk) MID2 MID2 1 7 Lucy Raymond
00114705 19377243-Pat? PubMed: Tarpey 2009 - - - - - - 0 for details contact Lucy Raymond (flr24 @ cam.ac.uk) - MRX101 Intellectual disability; for details please contact Lucy Raymond (flr24 @ cam.ac.uk) MID2 MID2 1 1 Lucy Raymond
00114706 - - - M no India - - 0 - - MRX101 Intellectual disability MID2 MID2 1 1 Thelma BK
00114707 - - - M - India - - 0 - - MRX101 Intellectual disability MID2 MID2 2 1 Thelma BK
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