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DO Term : FG syndrome [DOID:14711] Disease Ontology

Namespace  disease_ontology Obsolete  false
description  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.
  • synonyms:
  • ORDO:323,
  • 300422,
  • GARD:2317,
  • OMIM:300406,
  • Opitz-Kaveggia syndrome,
  • OMIM:300581,
  • UMLS_CUI:C0220769,
  • OMIM:305450,
  • OMIM:300321,
  • 300321,
  • ORDO:93932,
  • 305450,
  • 300406,
  • OMIM:300422,
  • 300581,
  • SNOMEDCT_US_2023_03_01:49984004,
  • MESH:C537923,
  • Keller syndrome
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Disease

Diseases --> Human genes

Diseases --> Mouse genes

Diseases --> Mouse models

Ontology

Ontology Term --> All ancestors

Ontology Term --> All descendants

Ontology Term --> Direct children

Ontology Term --> Direct parents