Disease #00092 (WARBM1 (Warburg micro syndrome, type 1 (WARBM1)), OMIM:600118)

Official abbreviation WARBM1
Name Warburg micro syndrome, type 1 (WARBM1)
OMIM ID 600118
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 3
Phenotype entries for this disease 2
Associated with 1 gene RAB3GAP1
Associated tissues -
Disease features -
Remarks -
Date created 2012-12-10 09:01:56 +01:00 (CET)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

3 entries on 1 page. Showing entries 1 - 3.
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00056408 - PubMed: Rump 2016 - F - - - - - - - WARBM1 Microcephaly (HP:0000252) - RAB3GAP1 1 1 Birgit Sikkema-Raddatz
00080941 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - WARBM1 Warburg micro syndrome 1 (OMIM:600118) RAB3GAP1 RAB3GAP1 1 1 Daniel Trujillano
00081093 - PubMed: Trujillano 2017 unaffected parents - - - - - - - - WARBM1 Warburg Micro syndrome 1 (OMIM:600118) RAB3GAP1 RAB3GAP1 1 1 Daniel Trujillano
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