Disease #04535 (ARTHS;MRD32 (Arboleda-Tham (ARTHS, previouslyMRD32)), OMIM:616268)

Official abbreviation ARTHS;MRD32
Name Arboleda-Tham (ARTHS, previouslyMRD32)
OMIM ID 616268
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 6
Phenotype entries for this disease 3
Associated with 1 gene KAT6A
Associated tissues -
Disease features -
Remarks -
Date created 2015-09-23 10:25:22 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

6 entries on 1 page. Showing entries 1 - 6.
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00081075 - PubMed: Trujillano 2017 unaffected non-carrier parents - - - - - - - - ARTHS;MRD32 Mental retardation, autosomal dominant 32 (OMIM:616268) KAT6A KAT6A 1 1 Daniel Trujillano
00383156 Case #1 - - F no Italy - - - - - ARTHS;MRD32 - - KAT6A 1 1 Vincenzo Nigro
00383157 - Case #2 - F no Italy - - - - - ARTHS;MRD32 - - KAT6A 1 1 Vincenzo Nigro
00408111 194485 - - M ? Germany - - - - - ARTHS;MRD32 - KAT6A KAT6A 1 1 Andreas Laner
00448515 286848 - - M no Germany - - - - - ARTHS;MRD32 Global developmental delay, Delayed speech and language development, Esodeviation KAT6A KAT6A 1 1 Andreas Laner
00470935 KAT6A_ARTHS2_Proband - - M no China - - - - - ARTHS;MRD32 Global developmental delay (HP:0001263); Severe expressive language delay (HP:0006868); Intellectual disability (HP:0001249); Abnormal social behavior (HP:0001263) KAT6A KAT6A 1 1 Haoyu Wang
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