Revesz syndrome
dyskeratosis congenita that has material basis in an X-linked recessive mutation of TINF2 on chromosome 14q12
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Revesz syndrome
Summary
Revesz syndrome is a head and neck disease[1]. It has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Revesz syndrome's instance of is recorded as head and neck disease[3].
- Revesz syndrome's instance of is recorded as developmental defect during embryogenesis[4].
- Revesz syndrome's instance of is recorded as rare disease[5].
- Revesz syndrome's instance of is recorded as class of disease[6].
- Revesz syndrome is a type of aplastic anemia[7].
- Revesz syndrome is a type of retinal disease[8].
- Revesz syndrome is a type of dyskeratosis congenita[9].
- Revesz syndrome is a type of hereditary retinal dystrophy[10].
- Revesz syndrome is a type of retinal cancer[11].
- Revesz syndrome is a type of autosomal dominant disease[12].
- Revesz syndrome's genetic association is recorded as TINF2[13].
- Revesz syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0070026[14].
- Revesz syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0070026[15].
- Revesz syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3088[16].
- Revesz syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[17].
Why It Matters
Revesz syndrome has Wikipedia articles in 6 language editions, a strong signal of global cultural recognition.[2] It is known by 13 alternative names across languages and contexts.[18]