OHVIRA
medical condition
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OHVIRA
Summary
OHVIRA is a developmental defect during embryogenesis[1]. OHVIRA draws 37 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #102 of 308).[2]
Key Facts
- OHVIRA's image is recorded as OHVIRA Ultrasound.jpg[3].
- OHVIRA's instance of is recorded as developmental defect during embryogenesis[4].
- OHVIRA's instance of is recorded as class of disease[5].
- OHVIRA's subclass of is recorded as uterine disease[6].
- OHVIRA's subclass of is recorded as renal agenesis[7].
- OHVIRA's subclass of is recorded as syndromic urogenital tract malformation[8].
- OHVIRA's subclass of is recorded as syndromic uterovaginal malformation[9].
- OHVIRA's subclass of is recorded as rare genetic gynecological and obstetrical diseases[10].
- OHVIRA's subclass of is recorded as syndromic renal or urinary tract malformation[11].
- OHVIRA's MeSH descriptor ID is recorded as C566010[12].
- OHVIRA's OMIM ID is recorded as 192050[13].
- OHVIRA's Orphanet ID is recorded as 3411[14].
- OHVIRA's UMLS CUI is recorded as C1860549[15].
- OHVIRA's UMLS CUI is recorded as C4302552[16].
- OHVIRA's GARD rare disease ID is recorded as 1910[17].
- OHVIRA's Mondo ID is recorded as MONDO_0008636[18].
Why It Matters
OHVIRA draws 37 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #102 of 308).[2] OHVIRA has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[19] OHVIRA is known by 10 alternative names across languages and contexts.[20]