FB2025_05 , released December 11, 2025
FB2025_05 , released December 11, 2025
CV Term Report
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General Information
Term Kenny-Caffey syndrome type 2 ID (Ontology) DOID:0080723 (Human Disease)
Definition A Kenny-Caffey syndrome that has_material_basis_in heterozygous mutation in the FAM111A gene on chromosome 11q12.
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autosomal genetic disease
 |__autosomal dominant disease__
syndrome                        |
osteochondrodysplasia           |
 |__Kenny-Caffey syndrome_______|
 |__Kenny-Caffey syndrome_______|
                                Kenny-Caffey syndrome type 2
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Is a autosomal dominant disease
Kenny-Caffey syndrome
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Synonyms
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GARD:83
MIM:127000
ORDO:93325