MCID: ISL027
MIFTS: 5

Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type

Categories: Metabolic diseases, Nephrological diseases, Rare diseases

Aliases & Classifications for Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type

MalaCards integrated aliases for Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type:

Name: Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type 60

Characteristics:

Orphanet epidemiological data:

60
isolated autosomal dominant hypomagnesemia, glaudemans type
Inheritance: Autosomal dominant; Prevalence: <1/1000000 (Worldwide); Age of onset: Infancy,Neonatal; Age of death: any age;

Classifications:



External Ids:

ICD10 via Orphanet 35 E83.4
Orphanet 60 ORPHA199326

Summaries for Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type

MalaCards based summary : Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type An important gene associated with Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type is KCNA1 (Potassium Voltage-Gated Channel Subfamily A Member 1).

Related Diseases for Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type

Symptoms & Phenotypes for Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type

Drugs & Therapeutics for Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type

Search Clinical Trials , NIH Clinical Center for Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type

Genetic Tests for Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type

Anatomical Context for Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type

Publications for Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type

Variations for Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type

Expression for Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type

Search GEO for disease gene expression data for Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type.

Pathways for Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type

GO Terms for Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type

Sources for Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
37 IUPHAR
38 KEGG
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43 MedGen
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46 MESH via Orphanet
47 MGI
50 NCI
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52 NDF-RT
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58 OMIM
59 OMIM via Orphanet
63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
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