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Disease Ontology Browser
SADDAN (DOID:0111158)
Alliance: disease page
Synonyms: SADDAN dysplasia; severe achondroplasia with developmental delay and acanthosis nigricans
Alt IDs: OMIM:616482, MESH:D000130, ORDO:85165, UMLS_CUI:C2674173
Definition: An autosomal dominant disease characterized by severe achondroplasia, developmental delay and acanthosis nigricans that has_material_basis_in heterozygous mutation in the FGFR3 gene on chromosome 4p16.


Contributing Projects:
Mouse Genome Database (MGD), Gene Expression Database (GXD), Mouse Models of Human Cancer database (MMHCdb) (formerly Mouse Tumor Biology (MTB), Gene Ontology (GO)
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last database update
12/03/2019
MGI 6.14
The Jackson Laboratory