Disease #06191 (BAGOS (Baker-Gordon syndrome), OMIM:618218)

Official abbreviation BAGOS
Name Baker-Gordon syndrome
OMIM ID 618218
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease 2
Phenotype entries for this disease 1
Associated with 1 gene SYT1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00409219 196814 - - M no Germany - - - - - BAGOS Neurodevelopmental delay, Autistic behavior, Absent speech, Developmental regression, Enuresis, Encopresis, Hypermetropia, Short stature, Hypotonia, neonatal SYT1 SYT1 1 1 Andreas Laner
00446556 - - - F no Spain white - - - - BAGOS - - SYT1 1 1 Francisco Martínez-Azorín
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