Disease #05986 (ODLURO (O'Donnell-Luria-Rodan syndrome), OMIM:618512)

Official abbreviation ODLURO
Name O'Donnell-Luria-Rodan syndrome
OMIM ID 618512
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 2
Associated with 1 gene MLL5
Associated tissues -
Disease features -
Remarks -
Date created 2021-11-08 09:24:31 +01:00 (CET)
Date last edited 2022-06-28 19:36:48 +02:00 (CEST)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00408116 195582 - - M ? Germany - - - - - ODLURO Macrocephaly, Absent speech, Global developmental delay, Abnormal muscle tone, Motor delay MLL5 MLL5 1 1 Andreas Laner
00434155 - - - M no Italy - - - - - ODLURO Speech delay, white matter alteration MLL5 MLL5 1 1 Pietro Palumbo
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