Kenny-Caffey syndrome

MONDO:0016516

A genetic condition characterized by long bone sclerosis and thickening, short stature, and head and eye anomalies. Many affected individuals have hypoparathyroidism with hypocalcemia.

Also known as: Kenny syndrome

4 clinical trials for this condition and its sub-types, 0 tagged with Kenny-Caffey syndrome itself.

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Where it sits in the disease tree

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Part of

↑ Syndromic disease (7133) ↑ Primordial dwarfism and slender bone disorder (9)

Sub-types of Kenny-Caffey syndrome

Autosomal recessive Kenny-Caffey syndrome 4 trials
Autosomal dominant Kenny-Caffey syndrome 0 trials

Including sub-types (4) Tagged with Kenny-Caffey syndrome (0)

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