Disease #00013 (Sialidosis (Neuraminidase Deficiency), OMIM:256550)

Official abbreviation Sialidosis
Name Neuraminidase Deficiency
OMIM ID 256550
Human Phenotype Ontology Project (HPO) HPO
Inheritance Autosomal recessive
Individuals reported having this disease 1
Phenotype entries for this disease 0
Associated with 1 gene NEU1
Associated tissues -
Disease features -
Remarks -


Individuals

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00000064 - M Iran yes - Sialidosis - NEU1 NEU1 1 1 Variome.ir
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