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 53 72
X-Linked Hypodontia 53

Classifications:



External Ids:

UMLS 72 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. An important gene associated with Hypodontia, X-Linked is EDA (Ectodysplasin A).

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

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. 38
20628232 2010
2
A novel missense mutation in the EDA gene associated with X-linked recessive isolated hypodontia. 38
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 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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