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 58

Characteristics:

Orphanet epidemiological data:

58
isolated autosomal dominant hypomagnesemia, glaudemans type
Inheritance: Autosomal dominant; Prevalence: <1/1000000 (Worldwide); Age of onset: Infancy,Neonatal; Age of death: any age;

Classifications:

Orphanet: 58  
Rare renal diseases
Inborn errors of metabolism


External Ids:

ICD10 via Orphanet 33 E83.4
Orphanet 58 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

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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
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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