# hypohidrotic ectodermal dysplasia

> no proof

**Wikidata**: [Q1077955](https://www.wikidata.org/wiki/Q1077955)  
**Wikipedia**: [English](https://en.wikipedia.org/wiki/Hypohidrotic_ectodermal_dysplasia)  
**Source**: https://4ort.xyz/entity/hypohidrotic-ectodermal-dysplasia


## References

1. Disease Ontology
2. Human Phenotype Ontology release 2018-03-08
3. Freebase Data Dumps. 2013
4. BBC Things
5. Detection of a molecular deletion at the DXS732 locus in a patient with X-linked hypohidrotic ectodermal dysplasia (EDA), with the identification of a unique junctional fragment.
6. A novel X-linked disorder of immune deficiency and hypohidrotic ectodermal dysplasia is allelic to incontinentia pigmenti and due to mutations in IKK-gamma (NEMO)
7. Mutations in the human homologue of mouse dl cause autosomal recessive and dominant hypohidrotic ectodermal dysplasia
8. [Identifiers.org](https://registry.identifiers.org/registry/doid)
9. [OpenAlex](https://docs.openalex.org/download-snapshot/snapshot-data-format)