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Xref MGI. OMIM mapping confirmed by DO. [SN].

AttributesValues
type
subClassOf
label
  • FG syndrome
comment
  • Xref MGI. OMIM mapping confirmed by DO. [SN].
described by
id
  • DOID:14711
database_cross_reference
  • ORDO:323
  • GARD:2317
  • MESH:C537923
  • OMIM:300321
  • OMIM:300406
  • OMIM:300422
  • OMIM:300581
  • OMIM:305450
  • ORDO:93932
  • SNOMEDCT_US_2021_09_01:49984004
  • UMLS_CUI:C0220769
has_exact_synonym
  • Keller syndrome (en)
  • Opitz-Kaveggia syndrome (en)
has_obo_namespace
  • disease_ontology
in_subset
http://purl.obolib...g/obo/IAO_0000115
  • A syndrome characterized by retardation, hyperactivity, hypotonia, broad thumbs, big first toes and a characteristic facial appearance including macrocephaly and has an X-linked recessive inheritance pattern.
is topic of
is annotatedSource of
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