Bjornstad syndrome
Human disease
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Bjornstad syndrome
Summary
Bjornstad syndrome is a developmental defect during embryogenesis[1]. It draws 27 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's subclass of is recorded as autosomal recessive disease[6].
- Bjornstad syndrome's subclass of is recorded as mitochondrial disorder due to a defect in assembly or maturation of the respiratory chain complexes[7].
- Bjornstad syndrome's subclass of is recorded as rare genetic developmental defect during embryogenesis[8].
- Bjornstad syndrome's subclass of is recorded as isolated genetic hair shaft abnormality[9].
- Bjornstad syndrome's subclass of is recorded as syndrome[10].
- Bjornstad syndrome's MeSH descriptor ID is recorded as C537633[11].
- Bjornstad syndrome's OMIM ID is recorded as 262000[12].
- Bjornstad syndrome's DiseasesDB is recorded as 33516[13].
- Bjornstad syndrome's Freebase ID is recorded as /m/04jfs6f[14].
- Bjornstad syndrome's KEGG ID is recorded as H00820[15].
- Bjornstad syndrome's Disease Ontology ID is recorded as DOID:0050677[16].
- Bjornstad syndrome's Orphanet ID is recorded as 123[17].
- Bjornstad syndrome's genetic association is recorded as BCS1L[18].
- Bjornstad syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050677[19].
- Bjornstad syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050677[20].
- Bjornstad syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_123[21].
- Bjornstad syndrome's UMLS CUI is recorded as C0266006[22].
- Bjornstad syndrome's GARD rare disease ID is recorded as 22[23].
- Bjornstad syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[24].
- Bjornstad syndrome's Mondo ID is recorded as MONDO_0009872[25].
- Bjornstad syndrome's Microsoft Academic ID is recorded as 2776552850[26].
- Bjornstad syndrome's Genetics Home Reference Conditions ID is recorded as bjornstad-syndrome[27].
Why It Matters
Bjornstad syndrome draws 27 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.[28] It is known by 11 alternative names across languages and contexts.[29]