Disease #02162 (ASPGX2 (Asperger syndrome X-linked 2), OMIM:300497)

Official abbreviation ASPGX2
Name Asperger syndrome X-linked 2
OMIM ID 300497
Human Phenotype Ontology Project (HPO) HPO
Inheritance X-linked
Individuals reported having this disease -
Phenotype entries for this disease -
Associated with 1 gene NLGN4X
Associated tissues -
Disease features -
Remarks -

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