Parietal foramina with cleidocranial dysplasia
human disease
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Parietal foramina with cleidocranial dysplasia
Summary
Parietal foramina with cleidocranial dysplasia is a developmental defect during embryogenesis[1].
Key Facts
- Parietal foramina with cleidocranial dysplasia's instance of is recorded as developmental defect during embryogenesis[2].
- Parietal foramina with cleidocranial dysplasia's instance of is recorded as rare disease[3].
- Parietal foramina with cleidocranial dysplasia's instance of is recorded as class of disease[4].
- Parietal foramina with cleidocranial dysplasia's subclass of is recorded as parietal foramina[5].
- Parietal foramina with cleidocranial dysplasia's subclass of is recorded as cleidocranial dysplasia[6].
- Parietal foramina with cleidocranial dysplasia's subclass of is recorded as cleidocranial dysplasia and isolated cranial ossification defect[7].
- Parietal foramina with cleidocranial dysplasia's subclass of is recorded as craniofacial disease[8].
- Parietal foramina with cleidocranial dysplasia's MeSH descriptor ID is recorded as C566825[9].
- Parietal foramina with cleidocranial dysplasia's OMIM ID is recorded as 168550[10].
- Parietal foramina with cleidocranial dysplasia's Orphanet ID is recorded as 251290[11].
- Parietal foramina with cleidocranial dysplasia's genetic association is recorded as MSX2[12].
- Parietal foramina with cleidocranial dysplasia's UMLS CUI is recorded as C1868597[13].
- Parietal foramina with cleidocranial dysplasia's ICD-10-CM is recorded as Q74.0[14].
- Parietal foramina with cleidocranial dysplasia's Mondo ID is recorded as MONDO_0008198[15].
- Parietal foramina with cleidocranial dysplasia's UniProt disease ID is recorded as DI-02132[16].