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DOID:0081441 - Nicolaides-Baraitser syndrome
Disease Ontology Definition:A syndrome that is characterized by severely impaired intellectual development, early-onset seizures, short stature, dysmorphic facial features, and sparse hair and that has_material_basis_in heterozygous mutation in the SMARCA2 gene on chromosome 9p24.
Synonyms: Intellectual disability-sparse hair-brachydactyly syndrome, SPARSE HAIR-IMPAIRED INTELLECTUAL DEVELOPMENT SYNDROME,
Xenbase Genes
:
Other Model Organisms: AGR, MGI, ZFIN, FlyBase, WormBase, RGD
Ontology Viewers: Disease Ontology, EMBL-EBI, OLSVis tree view, Ontobee
Parent(s):
autosomal dominant disease (is_a),
syndrome (is_a)