MCID: HYP196
MIFTS: 7

Hypodontia, X-Linked

Categories: Rare diseases

Aliases & Classifications for Hypodontia, X-Linked

MalaCards integrated aliases for Hypodontia, X-Linked:

Name: Hypodontia, X-Linked 52 71
X-Linked Hypodontia 52

Classifications:



External Ids:

UMLS 71 C2931428

Summaries for Hypodontia, X-Linked

MalaCards based summary : Hypodontia, X-Linked, also known as x-linked hypodontia, is related to ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive and ectodermal dysplasia. Affiliated tissues include skin.

Related Diseases for Hypodontia, X-Linked

Diseases related to Hypodontia, X-Linked via text searches within MalaCards or GeneCards Suite gene sharing:

# Related Disease Score Top Affiliating Genes
1 ectodermal dysplasia 10b, hypohidrotic/hair/tooth type, autosomal recessive 10.1
2 ectodermal dysplasia 10.1
3 erythrokeratoderma ''en cocardes'' 10.1
4 rare genetic skin disease 10.1

Symptoms & Phenotypes for Hypodontia, X-Linked

Drugs & Therapeutics for Hypodontia, X-Linked

Search Clinical Trials , NIH Clinical Center for Hypodontia, X-Linked

Genetic Tests for Hypodontia, X-Linked

Anatomical Context for Hypodontia, X-Linked

MalaCards organs/tissues related to Hypodontia, X-Linked:

40
Skin

Publications for Hypodontia, X-Linked

Articles related to Hypodontia, X-Linked:

# Title Authors PMID Year
1
A common founder mutation in the EDA-A1 gene in X-linked hypodontia. 61
20628232 2010
2
A novel missense mutation in the EDA gene associated with X-linked recessive isolated hypodontia. 61
18688569 2008

Variations for Hypodontia, X-Linked

Expression for Hypodontia, X-Linked

Search GEO for disease gene expression data for Hypodontia, X-Linked.

Pathways for Hypodontia, X-Linked

GO Terms for Hypodontia, X-Linked

Sources for Hypodontia, X-Linked

3 CDC
7 CNVD
9 Cosmic
10 dbSNP
11 DGIdb
17 EFO
18 ExPASy
19 FMA
28 GO
29 GTR
30 HMDB
31 HPO
32 ICD10
33 ICD10 via Orphanet
34 ICD9CM
35 IUPHAR
36 KEGG
37 LifeMap
39 LOVD
41 MedGen
43 MeSH
44 MESH via Orphanet
45 MGI
48 NCI
49 NCIt
50 NDF-RT
53 NINDS
54 Novoseek
56 OMIM
57 OMIM via Orphanet
61 PubMed
63 QIAGEN
68 SNOMED-CT via HPO
69 TGDB
70 Tocris
71 UMLS
72 UMLS via Orphanet
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