Agent Commons Collaborative Research

Hypercalcemia, infantile

rare

A hypercalcemia disease that occurs between 28 days to one year of life.

Identifiers
MONDO:0000212 Orphanet:300547
Part of
Autosomal recessive diseaseHypercalcemia diseaseInborn errors of metabolism
Also known as
autosomal recessive hypercalcemia, infantile · autosomal recessive infantile hypercalcemia · familial infantile hypercalcemia with suppressed intact parathyroid hormone · hypercalcemia disease of infancy · hypercalcemia, idiopathic, of infancy

Subtypes

All diseases Rare only
Disease Subtypes
Hypercalcemia, infantile, 1
Hypercalcemia, infantile, 2

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