MCID: CHL086
MIFTS: 11

Childhood Myocerebrohepatopathy Spectrum Disorders

Categories: Genetic diseases

Aliases & Classifications for Childhood Myocerebrohepatopathy Spectrum Disorders

MalaCards integrated aliases for Childhood Myocerebrohepatopathy Spectrum Disorders:

Name: Childhood Myocerebrohepatopathy Spectrum Disorders 24 29
Childhood Myocerebrohepatopathy Spectrum 25 69
Mchs 25

Classifications:



Summaries for Childhood Myocerebrohepatopathy Spectrum Disorders

Genetics Home Reference : 25 Childhood myocerebrohepatopathy spectrum, commonly called MCHS, is part of a group of conditions called the POLG-related disorders. The conditions in this group feature a range of similar signs and symptoms involving muscle-, nerve-, and brain-related functions. MCHS typically becomes apparent in children from a few months to 3 years old. People with this condition usually have problems with their muscles (myo-), brain (cerebro-), and liver (hepato-).

MalaCards based summary : Childhood Myocerebrohepatopathy Spectrum Disorders, also known as childhood myocerebrohepatopathy spectrum, is related to neuronitis and obesity. An important gene associated with Childhood Myocerebrohepatopathy Spectrum Disorders is POLG (DNA Polymerase Gamma, Catalytic Subunit). Affiliated tissues include liver and brain.

Related Diseases for Childhood Myocerebrohepatopathy Spectrum Disorders

Diseases related to Childhood Myocerebrohepatopathy Spectrum Disorders via text searches within MalaCards or GeneCards Suite gene sharing:

id Related Disease Score Top Affiliating Genes
1 neuronitis 10.0
2 obesity 9.8
3 thalassemia 9.8
4 thyroiditis 9.8

Symptoms & Phenotypes for Childhood Myocerebrohepatopathy Spectrum Disorders

Drugs & Therapeutics for Childhood Myocerebrohepatopathy Spectrum Disorders

Search Clinical Trials , NIH Clinical Center for Childhood Myocerebrohepatopathy Spectrum Disorders

Genetic Tests for Childhood Myocerebrohepatopathy Spectrum Disorders

Genetic tests related to Childhood Myocerebrohepatopathy Spectrum Disorders:

id Genetic test Affiliating Genes
1 Childhood Myocerebrohepatopathy Spectrum Disorders 29 24 POLG

Anatomical Context for Childhood Myocerebrohepatopathy Spectrum Disorders

MalaCards organs/tissues related to Childhood Myocerebrohepatopathy Spectrum Disorders:

39
Liver, Brain

Publications for Childhood Myocerebrohepatopathy Spectrum Disorders

Variations for Childhood Myocerebrohepatopathy Spectrum Disorders

Expression for Childhood Myocerebrohepatopathy Spectrum Disorders

Search GEO for disease gene expression data for Childhood Myocerebrohepatopathy Spectrum Disorders.

Pathways for Childhood Myocerebrohepatopathy Spectrum Disorders

GO Terms for Childhood Myocerebrohepatopathy Spectrum Disorders

Sources for Childhood Myocerebrohepatopathy Spectrum Disorders

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
16 ExPASy
18 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 MedGen
42 MeSH
43 MESH via Orphanet
44 MGI
46 NCI
47 NCIt
48 NDF-RT
51 NINDS
52 Novoseek
54 OMIM
55 OMIM via Orphanet
59 PubMed
60 QIAGEN
65 SNOMED-CT via HPO
66 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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