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syndromic neurometabolic disease with non-X-linked intellectual disability
?
TBD
human disease
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Subclasses
3
Smith–Lemli–Opitz syndrome
Recessive genetic condition
non-X-linked congenital disorder of glycosylation with intellectual disability as a major feature
human disease
combined oxidative phosphorylation defect type 27
human disease
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Instance of
class of disease
Subclass of
neurometabolic disease
genetic syndromic intellectual disability
Wikidata