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Human Disease

Nil-Deshwan neurodevelopmental syndrome

Term ID
DOID:0070652
Synonyms
Definition
A syndrome characterized by a range of congenital anomalies and central nervous system dysfunction, including global developmental delay, feeding difficulties, hypotonia, and impaired intellectual development that has_material_basis_in heterozygous mutation in the DOT1L gene on chromosome 19p13. (2)
References
Ontology
Human Disease   ( DOID:0070652 )
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Genes Involved
Zebrafish Models