Bjornstad syndrome
Human disease
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Bjornstad syndrome
Summary
Bjornstad syndrome is a developmental defect during embryogenesis[1]. It draws 59 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #117 of 308).[2]
Key Facts
- Bjornstad syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Bjornstad syndrome's instance of is recorded as rare disease[4].
- Bjornstad syndrome's instance of is recorded as class of disease[5].
- Bjornstad syndrome is a type of autosomal recessive disease[6].
- Bjornstad syndrome is a type of mitochondrial disorder due to a defect in assembly or maturation of the respiratory chain complexes[7].
- Bjornstad syndrome is a type of rare genetic developmental defect during embryogenesis[8].
- Bjornstad syndrome is a type of isolated genetic hair shaft abnormality[9].
- Bjornstad syndrome is a type of syndrome[10].
- Bjornstad syndrome's genetic association is recorded as BCS1L[11].
- Bjornstad syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050677[12].
- Bjornstad syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050677[13].
- Bjornstad syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_123[14].
- Bjornstad syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
Why It Matters
Bjornstad syndrome draws 59 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #117 of 308).[2] It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[16] It is known by 11 alternative names across languages and contexts.[17]