All diseases

OMIM ID
127000
OMIM term:
KENNY-CAFFEY SYNDROME, TYPE 2
Alternative terms:
KCS2
DWARFISM, CORTICAL THICKENING OF TUBULAR BONES, AND TRANSIENT HYPOCALCEMIA
KENNY SYNDROME
(∗) Location:
(†) Associated OMIM genes:
(‡) Associated MGI genes:

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