Idiopathic Infantile Hypercalcemia (IIH)

Alias:
Autosomal Recessive Infantile Hypercalcemia
Familial Infantile Hypercalcemia with Suppressed Intact Parathyroid Hormone
Vitamin D Hypersensitivity
Iih
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Idiopathic Infantile Hypercalcemia, also known as autosomal recessive infantile hypercalcemia, is related to hypercalcemia, infantile, 1 and nephrocalcinosis. An important gene associated with Idiopathic Infantile Hypercalcemia is SLC34A1 (Solute Carrier Family 34 Member 1), and among its related pathways/superpathways is FGF23 signaling in hypophosphatemic rickets and related disorders. The drugs Rifampicin and Anti-Bacterial Agents have been mentioned in the context of this disorder. Affiliated tissues include kidney and bone, and related phenotype is Increased shRNA abundance (Z-score > 2).
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AR
Newborn
<1/1000000
2
12
--

Medical Symptom

#
Categorization
Description
HPO Frequency
Orphanet Frequency
HPO Source Accession
No data available

Gene & Mutation

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Gene
Function
Score
Mutations
No data available

Related Drugs

Name
CAS Number
Status
Phase
No data available

Disease Model

Category
Name
MGI
Related Gene
Strain of Origin
Publications
No data available

References Literature

Title
PMID
Journal
Year
IF
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