FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
Help Close All Open All
General Information
Term orofaciodigital syndrome III ID (Ontology) DOID:0060373 (Human Disease)
Definition An orofaciodigital syndrome that is characterized by dysmorphic facies and severe intellectual deficits, and has_material_basis_in autosomal recessive inheritance.
Also Known As "Sugarman syndrome"
Comment
Links to External Ontologies
DO.org
Annotations
Records annotated with this term OR any of its CHILD TERMS
No relevant records available
Records annotated with this exact term (annotations to child terms are NOT included)
No relevant records available
show Full annotation statements including this term (annotations to child terms are NOT included), and relevant FlyBase records
No relevant statements available
Spanning Tree (Parents/Children)
Only view relationship:
autosomal genetic disease
 |__autosomal recessive disease__
syndrome                         |
 |__orofaciodigital syndrome_____|
                                 orofaciodigital syndrome III
Spanning Tree View Settings
Parents/Children
View Depth
Show hierarchy levels: for parents, for children
hide Relationships
Is a autosomal recessive disease
orofaciodigital syndrome
Part of
hide Synonyms & Secondary IDs
Synonyms
  • "Sugarman syndrome" EXACT
Secondary IDs
hide External Crossreferences & Linkouts
MESH:C557817
MIM:258850
ORDO:2752
SNOMEDCT_US_2023_03_01:239030004
UMLS_CUI:C0406726