MCID: CNG140
MIFTS: 6

Congenital Fibrosis of the Extraocular Muscles 1a

Categories: Genetic diseases

Aliases & Classifications for Congenital Fibrosis of the Extraocular Muscles 1a

MalaCards integrated aliases for Congenital Fibrosis of the Extraocular Muscles 1a:

Name: Congenital Fibrosis of the Extraocular Muscles 1a 24
Cfeom 1a 24
Cfeom1a 24

Classifications:



Summaries for Congenital Fibrosis of the Extraocular Muscles 1a

MalaCards based summary : Congenital Fibrosis of the Extraocular Muscles 1a, is also known as cfeom 1a.

Related Diseases for Congenital Fibrosis of the Extraocular Muscles 1a

Symptoms & Phenotypes for Congenital Fibrosis of the Extraocular Muscles 1a

Drugs & Therapeutics for Congenital Fibrosis of the Extraocular Muscles 1a

Search Clinical Trials , NIH Clinical Center for Congenital Fibrosis of the Extraocular Muscles 1a

Genetic Tests for Congenital Fibrosis of the Extraocular Muscles 1a

Genetic tests related to Congenital Fibrosis of the Extraocular Muscles 1a:

id Genetic test Affiliating Genes
1 Congenital Fibrosis of the Extraocular Muscles 1a 24

Anatomical Context for Congenital Fibrosis of the Extraocular Muscles 1a

Publications for Congenital Fibrosis of the Extraocular Muscles 1a

Variations for Congenital Fibrosis of the Extraocular Muscles 1a

Expression for Congenital Fibrosis of the Extraocular Muscles 1a

Search GEO for disease gene expression data for Congenital Fibrosis of the Extraocular Muscles 1a.

Pathways for Congenital Fibrosis of the Extraocular Muscles 1a

GO Terms for Congenital Fibrosis of the Extraocular Muscles 1a

Sources for Congenital Fibrosis of the Extraocular Muscles 1a

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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