Walker–Warburg syndrome
rare form of autosomal recessive congenital muscular dystrophy
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Walker–Warburg syndrome
Summary
Walker–Warburg syndrome is a rare disease[1]. It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Walker–Warburg syndrome's instance of is recorded as rare disease[3].
- Walker–Warburg syndrome's instance of is recorded as class of disease[4].
- Arthur Earl Walker is named after Walker–Warburg syndrome[5].
- Mette Warburg is named after Walker–Warburg syndrome[6].
- Walker–Warburg syndrome is a type of congenital muscular dystrophy[7].
- Walker–Warburg syndrome is a type of autosomal recessive[8].
- Walker–Warburg syndrome is a type of genetic disease[9].
- Walker–Warburg syndrome is a type of autosomal recessive disease[10].
- Walker–Warburg syndrome's NCI Thesaurus ID is recorded as C128118[11].
- Walker–Warburg syndrome's health specialty is recorded as ophthalmology[12].
- Walker–Warburg syndrome's health specialty is recorded as neurology[13].
- Walker–Warburg syndrome's health specialty is recorded as medical genetics[14].
- Walker–Warburg syndrome's genetic association is recorded as POMT1[15].
- Walker–Warburg syndrome's genetic association is recorded as POMGNT1[16].
- Walker–Warburg syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050560[17].
- Walker–Warburg syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050560[18].
- Walker–Warburg syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_588[19].
- Walker–Warburg syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_899[20].
- Walker–Warburg syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[21].
Why It Matters
Walker–Warburg syndrome has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2] It is known by 34 alternative names across languages and contexts.[22]