Disease #04624 (HJS1;MRD35 (Houge-Janssens syndrome, type 1), OMIM:616355)

Official abbreviation HJS1;MRD35
Name Houge-Janssens syndrome, type 1
OMIM ID 616355
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 5
Phenotype entries for this disease 3
Associated with 1 gene PPP2R5D
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:23 +02:00 (CEST)
Date last edited 2025-03-18 15:52:48 +01:00 (CET)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00080819 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - HJS1;MRD35 Mental retardation, autosomal dominant 35 (OMIM:616355) PPP2R5D MEA1, PPP2R5D 1 1 Daniel Trujillano
00306227 134 - - M - China - - - - - HJS1;MRD35 - PPP2R5D PPP2R5D 1 1 Sha Hong
00359336 163496 - - F - Hungary - - - - - HJS1;MRD35 exaggerated startle response, abnormality of movement PPP2R5D PPP2R5D 1 1 Andreas Laner
00464343 - - - - - - - - - - - HJS1;MRD35 - PPP2R5D PPP2R5D 1 1 Min Peng
00464344 - - - - - - - - - - - HJS1;MRD35 - PPP2R5D PPP2R5D 1 1 Min Peng
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