EEC syndrome
Information
- Disease name
- EEC syndrome
- Disease ID
- DOID:0060782
- Description
- "A syndrome characterized by ectrodactyly, ectodermal dysplasia, and orofacial clefts (cleft lip-palate)." [url:https\://rarediseases.info.nih.gov/diseases/2076/eec-syndrome]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT06412718 | Not yet recruiting | Validation of Human Drugs Target of Repurposed Drugs and Novel Therapies | May 2024 | April 2026 |
- Disase is a (Disease Ontology)
- DOID:225
- Cross Reference ID (Disease Ontology)
- MESH:C536189
- Cross Reference ID (Disease Ontology)
- NCI:C148261
- Cross Reference ID (Disease Ontology)
- ORDO:1896
- Cross Reference ID (Disease Ontology)
- SNOMEDCT_US_2023_03_01:39788007
- Cross Reference ID (Disease Ontology)
- UMLS_CUI:C0406704
- Exact Synonym (Disease Ontology)
- ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome
- Exact Synonym (Disease Ontology)
- ectrodactyly-ectodermal dysplasia-clefting syndrome
- Exact Synonym (Disease Ontology)
- Rudiger syndrome 1
- Exact Synonym (Disease Ontology)
- Walker-Clodius syndrome
- OrphaNumber from OrphaNet (Orphanet)
- 1896