Roberts syndrome
Human disease
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Roberts syndrome
Summary
Roberts syndrome is a rare disease[1]. It has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Roberts syndrome's instance of is recorded as rare disease[3].
- Roberts syndrome's instance of is recorded as class of disease[4].
- John Bingham Roberts is named after Roberts syndrome[5].
- Roberts syndrome is a type of autosomal recessive disease[6].
- Roberts syndrome is a type of SC phocomelia syndrome[7].
- Roberts syndrome is a type of syndrome[8].
- Roberts syndrome's Commons category is recorded as Roberts syndrome[9].
- Roberts syndrome's NCI Thesaurus ID is recorded as C126326[10].
- Roberts syndrome's NCI Thesaurus ID is recorded as C4681[11].
- Roberts syndrome's health specialty is recorded as medical genetics[12].
- Roberts syndrome's genetic association is recorded as ESCO2[13].
- Roberts syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_5325[14].
- Roberts syndrome's exact match is recorded as http://identifiers.org/doid/DOID:5325[15].
- Roberts syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
Roberts syndrome has Wikipedia articles in 9 language editions, a strong signal of global cultural recognition.[2] It is known by 10 alternative names across languages and contexts.[17]