Disease #02170 (BRNRS (syndrome, Brunner (BRNRS, monoamine oxidase A deficiency)), OMIM:300615)

Official abbreviation BRNRS
Name syndrome, Brunner (BRNRS, monoamine oxidase A deficiency)
OMIM ID 300615
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene MAOA
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Individuals

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00111408 S_114 PubMed: Popp 2017, Journal: Popp 2017 - M no ? (unknown) - - 0 - - BRNRS Male, 7 y, speech delay, moderate ID, behavioral anomalies (maternal XI 82%) MAOA MAOA 1 1 Bernt Popp
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