Disease #06421 (NECFM (Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination), OMIM:617393)

Official abbreviation NECFM
Name Neurodevelopmental disorder with epilepsy, cataracts, feeding difficulties, and delayed brain myelination
OMIM ID 617393
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal dominant
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene NACC1
Associated tissues -
Disease features -
Remarks -
Date created 2021-12-10 23:20:41 +01:00 (CET)
Date last edited N/A

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