Browse Rare Disease Information
The table below displays a list of all rare diseases contained within RARe-SOURCE™, their gene associations, links to related features within RARe-SOURCE™ and links to external data sources. Clicking on the disease name, lists all the disease aliases available in RARe-SOURCE™ for this disease as well as recent publications obtained from PubMed. Clicking on the associated gene lands on the ‘Gene Information’ page with specific details on the gene.
| Autosomal Dominant Hypohidrotic Ectodermal Dysplasia |
Disease Literature AI (46315) | GARD:
OMIM:
Orphanet:
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PubMed | |||
| Autosomal Recessive Hypohidrotic Ectodermal Dysplasia |
Disease Literature AI (18) | GARD:
OMIM:
Orphanet:
|
PubMed | |||
| Hidrotic Ectodermal Dysplasia |
Disease Literature AI (25986) | GARD:
OMIM:
Orphanet:
|
PubMed | |||
| Hypohidrotic Ectodermal Dysplasia With Immunodeficiency |
Disease Literature AI (49) | GARD:
OMIM:
Orphanet:
|
PubMed | |||
| Odonto-onycho-dermal Dysplasia |
Disease Literature AI (1465) | GARD:
OMIM:
Orphanet:
|
PubMed | |||
| Scalp-ear-nipple Syndrome |
Disease Literature AI (47) | GARD:
OMIM:
Orphanet:
|
PubMed | |||
| X-linked Hypohidrotic Ectodermal Dysplasia |
Disease Literature AI (823) | GARD:
OMIM:
Orphanet:
|
PubMed |