EDA-related ectodermal dysplasia
MONDO:1060241
Any ectodermal dysplasia syndrome in which the cause of the disease is a variation in the EDA gene. Key features are hypohidrosis and hypotrichosis; the condition is also characterized by skin anomalies such as soft, thin, and dry skin, eczema, and pigmentation anomalies, as well as fine or brittle hair, dental anomalies such as hypodontia or oligodontia, vocal hoarseness, and hyperthermia susceptibility.
Research intelligence
Directly mapped studies only · unique clinical trialsCurrent registry observations. Phase counts may overlap. Study start dates are not registry registration dates. Investigational interventions are not approved-treatment recommendations.
Medications under investigation
Verified disease and drug mappings that co-occur within the same study; not evidence of effectiveness.
MONDO disease family
Recruiting studies by city
Trial status
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Study start year
Investigated drug interventions
Drugs being studied
Disease identity and terminology: MONDO. Trial relationships: ClinicalTrials.gov.