MCID: ECT012
MIFTS: 3

Ectodermal Dysplasia Alopecia Preaxial Polydactyly

Categories: Rare diseases

Aliases & Classifications for Ectodermal Dysplasia Alopecia Preaxial Polydactyly

MalaCards integrated aliases for Ectodermal Dysplasia Alopecia Preaxial Polydactyly:

Name: Ectodermal Dysplasia Alopecia Preaxial Polydactyly 52 71
Absence of Body & Scalp Hair, Rounded Nails, Thin Dental Enamel, Preaxial Polydactyly of the Feet, and Unusual Facial Appearance 52

Classifications:



External Ids:

UMLS 71 C2931691

Summaries for Ectodermal Dysplasia Alopecia Preaxial Polydactyly

MalaCards based summary : Ectodermal Dysplasia Alopecia Preaxial Polydactyly, is also known as absence of body & scalp hair, rounded nails, thin dental enamel, preaxial polydactyly of the feet, and unusual facial appearance.

Related Diseases for Ectodermal Dysplasia Alopecia Preaxial Polydactyly

Symptoms & Phenotypes for Ectodermal Dysplasia Alopecia Preaxial Polydactyly

Drugs & Therapeutics for Ectodermal Dysplasia Alopecia Preaxial Polydactyly

Search Clinical Trials , NIH Clinical Center for Ectodermal Dysplasia Alopecia Preaxial Polydactyly

Genetic Tests for Ectodermal Dysplasia Alopecia Preaxial Polydactyly

Anatomical Context for Ectodermal Dysplasia Alopecia Preaxial Polydactyly

Publications for Ectodermal Dysplasia Alopecia Preaxial Polydactyly

Variations for Ectodermal Dysplasia Alopecia Preaxial Polydactyly

Expression for Ectodermal Dysplasia Alopecia Preaxial Polydactyly

Search GEO for disease gene expression data for Ectodermal Dysplasia Alopecia Preaxial Polydactyly.

Pathways for Ectodermal Dysplasia Alopecia Preaxial Polydactyly

GO Terms for Ectodermal Dysplasia Alopecia Preaxial Polydactyly

Sources for Ectodermal Dysplasia Alopecia Preaxial Polydactyly

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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