MCID: CTK001
MIFTS: 7

Cote Katsantoni Syndrome

Categories: Bone diseases, Rare diseases

Aliases & Classifications for Cote Katsantoni Syndrome

MalaCards integrated aliases for Cote Katsantoni Syndrome:

Name: Cote Katsantoni Syndrome 54 74
Ectodermal Dysplasia Osteosclerosis 54

Classifications:



External Ids:

UMLS 74 C2931195

Summaries for Cote Katsantoni Syndrome

MalaCards based summary : Cote Katsantoni Syndrome, also known as ectodermal dysplasia osteosclerosis, is related to ectodermal dysplasia and neutropenia.

Related Diseases for Cote Katsantoni Syndrome

Diseases related to Cote Katsantoni Syndrome via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 ectodermal dysplasia 10.1
2 neutropenia 10.1
3 atrial heart septal defect 10.1

Symptoms & Phenotypes for Cote Katsantoni Syndrome

Drugs & Therapeutics for Cote Katsantoni Syndrome

Search Clinical Trials , NIH Clinical Center for Cote Katsantoni Syndrome

Genetic Tests for Cote Katsantoni Syndrome

Anatomical Context for Cote Katsantoni Syndrome

Publications for Cote Katsantoni Syndrome

Articles related to Cote Katsantoni Syndrome:

# Title Authors Year
1
Ectodermal dysplasia, osteosclerosis, atrial septal defect, malabsorption, neutropenia, growth, and mental retardation: the CA'tAc-Katsantoni syndrome? ( 3565486 )
1987

Variations for Cote Katsantoni Syndrome

Expression for Cote Katsantoni Syndrome

Search GEO for disease gene expression data for Cote Katsantoni Syndrome.

Pathways for Cote Katsantoni Syndrome

GO Terms for Cote Katsantoni Syndrome

Sources for Cote Katsantoni Syndrome

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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