Howel–Evans syndrome
Tylosis with oesophageal cancer
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Howel–Evans syndrome
Summary
Howel–Evans syndrome is a rare disease[1]. It draws 398 Wikipedia views per month (rare_disease category, ranking #231 of 627).[2]
Key Facts
- Howel–Evans syndrome's instance of is recorded as rare disease[3].
- Howel–Evans syndrome's instance of is recorded as class of disease[4].
- Howel–Evans syndrome is a type of palmoplantar keratosis[5].
- Howel–Evans syndrome is a type of esophageal cancer[6].
- Howel–Evans syndrome is a type of autosomal dominant disease associated with focal palmoplantar keratoderma as a major feature[7].
- Howel–Evans syndrome is a type of rare gastroesophageal disease[8].
- Howel–Evans syndrome is a type of genetic gastro-esophageal disease[9].
- Howel–Evans syndrome is a type of syndrome[10].
- Howel–Evans syndrome is a type of autosomal dominant disease[11].
- Howel–Evans syndrome's health specialty is recorded as medical genetics[12].
- Howel–Evans syndrome's genetic association is recorded as RHBDF2[13].
- Howel–Evans syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2198[14].
- Howel–Evans syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111506[15].
- Howel–Evans syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111506[16].
Why It Matters
Howel–Evans syndrome draws 398 Wikipedia views per month (rare_disease category, ranking #231 of 627).[2] It is known by 23 alternative names across languages and contexts.[17]