CTRCT27
MCID: CTR178
MIFTS: 17

Cataract 27 (CTRCT27)

Categories: Eye diseases, Fetal diseases, Genetic diseases, Metabolic diseases, Nephrological diseases, Neuronal diseases, Oral diseases, Rare diseases

Aliases & Classifications for Cataract 27

MalaCards integrated aliases for Cataract 27:

Name: Cataract 27 58 12
Ctrct27 58 12
Cataract 27, Nuclear Progressive 58
Cataract 27 Nuclear Progressive 12
Cataract, Nuclear Progressive 74
Ccnp 58

Classifications:



External Ids:

Disease Ontology 12 DOID:0110233
OMIM 58 607304
ICD10 34 Q12.0
MedGen 43 C1846520
UMLS 74 C1846520

Summaries for Cataract 27

Disease Ontology : 12 A cataract that has material basis in mutation in the region 2p12.

MalaCards based summary : Cataract 27, also known as ctrct27, is related to cataract. An important gene associated with Cataract 27 is CTRCT27 (Cataract, Congenital, Nuclear Progressive). Affiliated tissues include eye.

Description from OMIM: 607304

Related Diseases for Cataract 27

Symptoms & Phenotypes for Cataract 27

Clinical features from OMIM:

607304

Drugs & Therapeutics for Cataract 27

Search Clinical Trials , NIH Clinical Center for Cataract 27

Genetic Tests for Cataract 27

Anatomical Context for Cataract 27

MalaCards organs/tissues related to Cataract 27:

42
Eye

Publications for Cataract 27

Variations for Cataract 27

Expression for Cataract 27

Search GEO for disease gene expression data for Cataract 27.

Pathways for Cataract 27

GO Terms for Cataract 27

Sources for Cataract 27

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
20 FMA
29 GO
30 GTR
31 HGMD
32 HMDB
33 HPO
34 ICD10
35 ICD10 via Orphanet
36 ICD9CM
37 IUPHAR
38 KEGG
39 LifeMap
41 LOVD
43 MedGen
45 MeSH
46 MESH via Orphanet
47 MGI
50 NCI
51 NCIt
52 NDF-RT
55 NINDS
56 Novoseek
58 OMIM
59 OMIM via Orphanet
63 PubMed
65 QIAGEN
70 SNOMED-CT via HPO
71 SNOMED-CT via Orphanet
72 TGDB
73 Tocris
74 UMLS
75 UMLS via Orphanet
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