Disease #06882 (VIBOS (Vissers-Bodmer syndrome), OMIM:619033)

Official abbreviation VIBOS
Name Vissers-Bodmer syndrome
OMIM ID 619033
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 CNOT1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-13 14:57:26 +01:00 (CET)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00395419 188611 - - M no Germany - - - - - VIBOS Macrocephaly, Global developmental delay, Abnormal facial shape CNOT1 CNOT1 1 1 Andreas Laner
00472217 - Verebi et al. (submitted) - F - France - - - - - VIBOS Myopathy - CNOT1 1 1 Camille Verebi
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