Bowen-Conradi syndrome
Human disease
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Bowen-Conradi syndrome
Summary
Bowen-Conradi syndrome is a developmental defect during embryogenesis[1]. It draws 21 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #132 of 308).[2]
Key Facts
- Bowen-Conradi syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Bowen-Conradi syndrome's instance of is recorded as rare disease[4].
- Bowen-Conradi syndrome's instance of is recorded as class of disease[5].
- Bowen-Conradi syndrome is a type of autosomal recessive disease[6].
- Bowen-Conradi syndrome is a type of syndrome with microcephaly as major feature[7].
- Bowen-Conradi syndrome is a type of multiple congenital anomalies/dysmorphic syndrome-intellectual disability[8].
- Bowen-Conradi syndrome is a type of genetic syndromic intellectual disability[9].
- Bowen-Conradi syndrome is a type of syndrome[10].
- Bowen-Conradi syndrome's ICD-9-CM is recorded as 759.89[11].
- Bowen-Conradi syndrome's genetic association is recorded as EMG1[12].
- Bowen-Conradi syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050684[13].
- Bowen-Conradi syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050684[14].
- Bowen-Conradi syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1270[15].
- Bowen-Conradi syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
Bowen-Conradi syndrome draws 21 Wikipedia views per month (developmental_defect_during_embryogenesis category, ranking #132 of 308).[2] It is known by 12 alternative names across languages and contexts.[17]