anencephaly
Information
- Disease name
- anencephaly
- Disease ID
- DOID:0060668
- Description
- "A congenital nervous system abnormality characterized by failure of the anterior neuropore to close resulting in partial or complete absence of the cranial vault accompanied by absence of overlying tissues, including the brain and cerebral hemispheres, skull and scalp." [url:https\://en.wikipedia.org/wiki/Anencephaly, url:https\://ghr.nlm.nih.gov/condition/anencephaly]
Disease area statistics
[No Data.]
Chromosome band
[No Data.]
Annotation
| Genes | Mutation | Description | Source | Links |
|---|
| NCT ID | Status | Phase | Summary | Start date | Completion date |
|---|---|---|---|---|---|
| NCT00636233 | Completed | Genetics of Spina Bifida and Anencephaly | May 1993 | August 2, 2017 | |
| NCT00031122 | Unknown status | Study of Genetic Risk Factors for Spina Bifida and Anencephaly | September 2000 | September 2012 |
- Disase is a (Disease Ontology)
- DOID:2490
- Cross Reference ID (Disease Ontology)
- GARD:5808
- Cross Reference ID (Disease Ontology)
- ICD10CM:Q00.0
- Cross Reference ID (Disease Ontology)
- MESH:D000757
- Cross Reference ID (Disease Ontology)
- MIM:206500
- Cross Reference ID (Disease Ontology)
- ORDO:1048
- HPO Human Phenotype ID (Human Phenotype Ontology)
- HP:0002323
- ICD10 preferred id (Insert disease from ICD10)
- D0013521
- ICD10 class code (Insert disease from ICD10)
- Q00.0
- MeSH unique ID (MeSH (Medical Subject Headings))
- D000757