Disease #05950 (NEDBA (neurodevelopmental disorder with/without variable brain abnormalities (NEDBA)), OMIM:618443)

Official abbreviation NEDBA
Name neurodevelopmental disorder with/without variable brain abnormalities (NEDBA)
OMIM ID 618443
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 MAPK8IP3
Associated tissues -
Disease features -
Remarks -
Date created 2021-06-23 17:23:30 +02:00 (CEST)
Date last edited 2021-12-10 21:51:32 +01:00 (CET)


Individuals

2 entries on 1 page. Showing entries 1 - 2.
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00391223 187184 - - M no Germany - - - - - NEDBA Thick eyebrow, Autistic behavior, Autism with high cognitive abilities, Goiter, Long hallux, Sandal gap, Truncal obesity, Clumsiness, Highly arched eyebrow, Large earlobe MAPK8IP3 MAPK8IP3 1 1 Andreas Laner
00436279 269025 - - F no ? (unknown) - - - - - NEDBA Intellectual disability, Increased body weight, EEG abnormality, EEG with spike-wave complexes, Abnormal repetitive mannerisms, Hyperactivity, Delayed speech and language development, Neurodevelopmental delay MAPK8IP3 MAPK8IP3 1 1 Andreas Laner
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