MCID: CTK001
MIFTS: 9

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 53 73
Ectodermal Dysplasia Osteosclerosis 53

Classifications:



External Ids:

UMLS 73 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. Affiliated tissues include bone and heart.

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

MalaCards organs/tissues related to Cote Katsantoni Syndrome:

41
Bone, Heart

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 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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