Hypocalcemia, Autosomal Dominant 1 (HYPOC1)

Alias:
Autosomal Dominant Hypocalcemia
Autosomal Dominant Hypocalcemia 1
Hypoc1
Hypocalcemia, Autosomal Dominant, with Bartter Syndrome
Hypocalcemia, Autosomal Dominant
Hypercalciuric Hypocalcemia
Familial Hypocalcemia
Ad Hypocalcemia
Hypocalcemia, Autosomal Dominant, Bartter Syndrome Incl.
Autosomal Dominant Hypocalcemia with Bartter Syndrome
Hypoparathyroidism - Autosomal Dominant
Autosomal Dominant Hypoparathyroidism
Familial Hypercalciuric Hypocalcemia
Bartter Syndrome with Hypocalcemia
Hypocalcemia, Familial
Hypocalcemia
Hypoc
Adh
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Basic Information
Medical Symptom
Gene & Mutation
Related Drugs
Disease Model
References Literature
Hypocalcemia, Autosomal Dominant 1, also known as autosomal dominant hypocalcemia, is related to hyperparathyroidism, neonatal severe and hypophosphatemic rickets, autosomal dominant, and has symptoms including muscle cramp, seizures and carpopedal spasm. An important gene associated with Hypocalcemia, Autosomal Dominant 1 is CASR (Calcium Sensing Receptor), and among its related pathways/superpathways are Signal Transduction and GPCR downstream signalling. The drugs Zoledronic acid and Foscarnet have been mentioned in the context of this disorder. Affiliated tissues include kidney and eye, and related phenotypes are emotional lability and depression
Related ID:

Basic Information

Inheritance
Age of Onset
Prevalence
Related Gene
Related Mouse Models
Reference
MALACARDS
AD
All ages
1-9/100000
22
217
144

Medical Symptom

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

Gene & Mutation

#
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
No Data Found!
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