Disease #07128 (NEDFSAB (neurodevelopmental disorder with dysmorphic facies, absent speech and ambulation, and brain abnormalities), OMIM:621012)

Official abbreviation NEDFSAB
Name neurodevelopmental disorder with dysmorphic facies, absent speech and ambulation, and brain abnormalities
OMIM ID 621012
Human Phenotype Ontology Project (HPO) HPO
Inheritance -
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene CHASERR
Associated tissues -
Disease features -
Remarks -
Date created 2024-11-22 19:18:55 +01:00 (CET)
Date last edited N/A

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