Aliases & Classifications for Sella Turcica, Bridged

MalaCards integrated aliases for Sella Turcica, Bridged:

Name: Sella Turcica, Bridged 57

Characteristics:

OMIM:

57
Inheritance:
autosomal dominant


HPO:

32
sella turcica, bridged:
Inheritance autosomal dominant inheritance


External Ids:

OMIM 57 182200
MedGen 42 C1866959

Summaries for Sella Turcica, Bridged

MalaCards based summary : Sella Turcica, Bridged is related to myopathy and 47,xyy. Related phenotype is bridged sella turcica.

More information from OMIM: 182200

Related Diseases for Sella Turcica, Bridged

Diseases related to Sella Turcica, Bridged via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 myopathy 10.1
2 47,xyy 10.1

Symptoms & Phenotypes for Sella Turcica, Bridged

Human phenotypes related to Sella Turcica, Bridged:

32
# Description HPO Frequency HPO Source Accession
1 bridged sella turcica 32 HP:0005449

Symptoms via clinical synopsis from OMIM:

57
Skull:
bridged sella turcica

Radiology:
osseous bridging of anterior and posterior clinoids

Clinical features from OMIM:

182200

Drugs & Therapeutics for Sella Turcica, Bridged

Search Clinical Trials , NIH Clinical Center for Sella Turcica, Bridged

Genetic Tests for Sella Turcica, Bridged

Anatomical Context for Sella Turcica, Bridged

Publications for Sella Turcica, Bridged

Articles related to Sella Turcica, Bridged:

# Title Authors PMID Year
1
Osteogenesis imperfecta in twenty-three members of a kindred with heritable features contributed by a non-specific skeletal disorder. 8
5676881 1968

Variations for Sella Turcica, Bridged

Expression for Sella Turcica, Bridged

Search GEO for disease gene expression data for Sella Turcica, Bridged.

Pathways for Sella Turcica, Bridged

GO Terms for Sella Turcica, Bridged

Sources for Sella Turcica, Bridged

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 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 TGDB
71 Tocris
72 UMLS
73 UMLS via Orphanet
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