Autosomal Dominant Kenny-Caffey Syndrome
| Disease Aliases (9) | Dwarfism, cortical thickening of tubular bones, and transient hypocalcemia Dwarfism, cortical thickening of tubular bones and transient hypocalcemia Kcs2 Kenny syndrome Kenny-caffey syndrome type 2 Kenny-caffey syndrome, autosomal dominant Kenny-caffey syndrome, type 2 Kenny-caffey syndrome, type 2; kcs2 |
Associated Genes (1) NCBI-RefSeq: FAM111A (FAM111 trypsin like peptidase A) External Links: gnomAD browser Ensembl GeneCards
| |||||||
| Cross-references of Autosomal dominant Kenny-Caffey syndrome | OMIM | GARD | Orphanet | NCBI-GTR | NCBI-MedGen | MalaCards | MeSH | Annotations | |