MCID: ISL027
MIFTS: 5

Isolated Autosomal Dominant Hypomagnesemia, Glaudemans Type

Categories: Nephrological diseases, Metabolic 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 59

Characteristics:

Orphanet epidemiological data:

59
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:

Orphanet 59 ORPHA199326
ICD10 via Orphanet 34 E83.4

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 ExPASy
19 FMA
28 GO
29 GTR
30 HGMD
31 HMDB
32 HPO
33 ICD10
34 ICD10 via Orphanet
35 ICD9CM
36 IUPHAR
37 KEGG
38 LifeMap
40 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
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54 NINDS
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58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
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