Yunis-Varon syndrome
Human disease
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Yunis-Varon syndrome
Summary
Yunis-Varon syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Yunis-Varon syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Yunis-Varon syndrome's instance of is recorded as rare disease[4].
- Yunis-Varon syndrome's instance of is recorded as class of disease[5].
- Yunis-Varon syndrome is a type of syndrome[6].
- Yunis-Varon syndrome is a type of cleidocranial dysplasia and isolated cranial ossification defect[7].
- Yunis-Varon syndrome is a type of genetic disease[8].
- Yunis-Varon syndrome is a type of autosomal recessive disease[9].
- Yunis-Varon syndrome's health specialty is recorded as medical genetics[10].
- Yunis-Varon syndrome's genetic association is recorded as FIG4[11].
- Yunis-Varon syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060589[12].
- Yunis-Varon syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060589[13].
- Yunis-Varon syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3472[14].
- Yunis-Varon syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
Yunis-Varon syndrome has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2] It is known by 9 alternative names across languages and contexts.[16]