MCID: CTR178
MIFTS: 18

Cataract 27

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

Aliases & Classifications for Cataract 27

MalaCards integrated aliases for Cataract 27:

Name: Cataract 27 57 12 15
Ctrct27 57 12
Cataract 27, Nuclear Progressive 57
Cataract 27 Nuclear Progressive 12
Cataract, Nuclear Progressive 73
Ccnp 57

Classifications:



External Ids:

OMIM 57 607304
Disease Ontology 12 DOID:0110233
ICD10 33 Q12.0
MedGen 42 C1846520
UMLS 73 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:

41
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 ExPASy
19 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 LOVD
42 MedGen
44 MeSH
45 MESH via Orphanet
46 MGI
49 NCI
50 NCIt
51 NDF-RT
54 NINDS
55 Novoseek
57 OMIM
58 OMIM via Orphanet
62 PubMed
64 QIAGEN
69 SNOMED-CT via HPO
70 SNOMED-CT via Orphanet
71 TGDB
72 Tocris
73 UMLS
74 UMLS via Orphanet
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