Disease #07067 (NEDEPH (neurodevelopmental disorder with epilepsy and hemochromatosis), OMIM:301072)

Official abbreviation NEDEPH
Name neurodevelopmental disorder with epilepsy and hemochromatosis
OMIM ID 301072
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease 1
Phenotype entries for this disease 1
Associated with 1 gene PIGA
Associated tissues -
Disease features -
Remarks -
Date created 2024-02-02 17:32:25 +01:00 (CET)
Date last edited N/A


Individuals

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00448512 286520 - - M no Germany - - - - - NEDEPH Delayed gross motor development, Neurodevelopmental delay, Abnormal visual fixation, Focal-onset seizure, Febrile status epilepticus, Esodeviation, Large for gestational age, EEG abnormality, Hypomethioninemia PIGA PIGA 1 1 Andreas Laner
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