FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Crouzon syndrome-acanthosis nigricans syndrome ID (Ontology) DOID:0111161 (Human Disease)
Definition A syndrome characterized by Crouzon-like features, premature synostosis of cranial sutures, and acanthosis nigricans that has_material_basis_in heterozygous missense mutation in the FGFR3 gene on chromosome 4p16.
Also Known As "CAN" ; "Crouzon-dermoskeletal syndrome" ; "Crouzonodermoskeletal syndrome"
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DO.org
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 Genes
 Crouzon syndrome-acanthosis nigricans syndrome       1
 for disease ribbon | Crouzon syndrome-acanthosis nigricans syndrome       1
 model of | Crouzon syndrome-acanthosis nigricans syndrome       1
Spanning Tree (Parents/Children)
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autosomal genetic disease
 |__autosomal dominant disease__
disease                         |
 |__syndrome____________________|
connective tissue disease       |
 |__bone disease________________|
                                Crouzon syndrome-acanthosis nigricans syndrome  1 rec.
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Is a autosomal dominant disease
bone disease
syndrome
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Synonyms
  • "CAN" EXACT OMO:0003012
    "Crouzon-dermoskeletal syndrome" EXACT
    "Crouzonodermoskeletal syndrome" EXACT
Secondary IDs
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MIM:612247
ORDO:93262