MCID: TBK001
MIFTS: 7

Teebi Kaurah Syndrome

Categories: Rare diseases

Aliases & Classifications for Teebi Kaurah Syndrome

MalaCards integrated aliases for Teebi Kaurah Syndrome:

Name: Teebi Kaurah Syndrome 49 69
Total Anonychia Congenita and Microcephaly with Normal Intelligence 49

Classifications:



External Ids:

UMLS 69 C2931373

Summaries for Teebi Kaurah Syndrome

MalaCards based summary : Teebi Kaurah Syndrome, also known as total anonychia congenita and microcephaly with normal intelligence, is related to anonychia, total, with microcephaly and nail disorder, nonsyndromic congenital, 4.

Related Diseases for Teebi Kaurah Syndrome

Diseases related to Teebi Kaurah Syndrome via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 anonychia, total, with microcephaly 11.3
2 nail disorder, nonsyndromic congenital, 4 10.2
3 microcephaly 10.2

Symptoms & Phenotypes for Teebi Kaurah Syndrome

Drugs & Therapeutics for Teebi Kaurah Syndrome

Search Clinical Trials , NIH Clinical Center for Teebi Kaurah Syndrome

Genetic Tests for Teebi Kaurah Syndrome

Anatomical Context for Teebi Kaurah Syndrome

Publications for Teebi Kaurah Syndrome

Articles related to Teebi Kaurah Syndrome:

# Title Authors Year
1
Total anonychia congenita and microcephaly with normal intelligence: a new autosomal-recessive syndrome? ( 8985482 )
1996

Variations for Teebi Kaurah Syndrome

Expression for Teebi Kaurah Syndrome

Search GEO for disease gene expression data for Teebi Kaurah Syndrome.

Pathways for Teebi Kaurah Syndrome

GO Terms for Teebi Kaurah Syndrome

Sources for Teebi Kaurah Syndrome

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
16 ExPASy
18 FMA
27 GO
28 GTR
29 HGMD
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 MedGen
41 MeSH
42 MESH via Orphanet
43 MGI
45 NCI
46 NCIt
47 NDF-RT
50 NINDS
51 Novoseek
53 OMIM
54 OMIM via Orphanet
58 PubMed
60 QIAGEN
65 SNOMED-CT via HPO
66 SNOMED-CT via Orphanet
67 TGDB
68 Tocris
69 UMLS
70 UMLS via Orphanet
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