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Disease Ontology Browser
Catel Manzke syndrome (DOID:0081122)
Alliance: disease page
Synonyms: Hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome; Micrognathia digital syndrome
Alt IDs: OMIM:616145, MESH:C535347, ORDO:1388
Definition: A bone disease that is characterized by the Pierre Robin anomaly, which comprises cleft palate, glossoptosis, and micrognathia, and a unique form of bilateral hyperphalangy in which there is an accessory bone inserted between the second metacarpal and its corresponding proximal phalanx, resulting in radial deviation of the index finger and that has_material_basis_in homozygous or compound heterozygous mutation in the TGDS gene on chromosome 13q32.

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
MGI 6.22
The Jackson Laboratory