MCID: PHX001
MIFTS: 5

Phox2a-Related Congenital Fibrosis of the Extraocular Muscles malady

Categories: Genetic diseases

Aliases & Classifications for Phox2a-Related Congenital Fibrosis of the Extraocular Muscles

Aliases & Descriptions for Phox2a-Related Congenital Fibrosis of the Extraocular Muscles:

Name: Phox2a-Related Congenital Fibrosis of the Extraocular Muscles 24

Classifications:



Summaries for Phox2a-Related Congenital Fibrosis of the Extraocular Muscles

MalaCards based summary : Phox2a-Related Congenital Fibrosis of the Extraocular Muscles An important gene associated with Phox2a-Related Congenital Fibrosis of the Extraocular Muscles is PHOX2A (Paired Like Homeobox 2a).

Related Diseases for Phox2a-Related Congenital Fibrosis of the Extraocular Muscles

Symptoms & Phenotypes for Phox2a-Related Congenital Fibrosis of the Extraocular Muscles

Drugs & Therapeutics for Phox2a-Related Congenital Fibrosis of the Extraocular Muscles

Search Clinical Trials , NIH Clinical Center for Phox2a-Related Congenital Fibrosis of the Extraocular Muscles

Genetic Tests for Phox2a-Related Congenital Fibrosis of the Extraocular Muscles

Genetic tests related to Phox2a-Related Congenital Fibrosis of the Extraocular Muscles:

id Genetic test Affiliating Genes
1 Phox2a-Related Congenital Fibrosis of the Extraocular Muscles 24 PHOX2A

Anatomical Context for Phox2a-Related Congenital Fibrosis of the Extraocular Muscles

Publications for Phox2a-Related Congenital Fibrosis of the Extraocular Muscles

Variations for Phox2a-Related Congenital Fibrosis of the Extraocular Muscles

Expression for Phox2a-Related Congenital Fibrosis of the Extraocular Muscles

Search GEO for disease gene expression data for Phox2a-Related Congenital Fibrosis of the Extraocular Muscles.

Pathways for Phox2a-Related Congenital Fibrosis of the Extraocular Muscles

GO Terms for Phox2a-Related Congenital Fibrosis of the Extraocular Muscles

Sources for Phox2a-Related Congenital Fibrosis of the Extraocular Muscles

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
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42 MeSH
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44 MGI
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48 NDF-RT
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52 Novoseek
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55 OMIM via Orphanet
59 PubMed
60 QIAGEN
65 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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