congenital insensitivity to pain
0 sources
congenital insensitivity to pain
Summary
congenital insensitivity to pain is a rare disease[1]. It ranks in the top 7% of rare_disease entities by monthly Wikipedia readership (649 views/month).[2]
Key Facts
- congenital insensitivity to pain's instance of is recorded as rare disease[3].
- congenital insensitivity to pain's instance of is recorded as disease[4].
- congenital insensitivity to pain's subclass of is recorded as absence of pain sensation[5].
- congenital insensitivity to pain's MeSH descriptor ID is recorded as D000699[6].
- congenital insensitivity to pain's OMIM ID is recorded as 243000[7].
- congenital insensitivity to pain's OMIM ID is recorded as 147430[8].
- congenital insensitivity to pain's DiseasesDB is recorded as 31214[9].
- congenital insensitivity to pain's Freebase ID is recorded as /m/02wljd[10].
- congenital insensitivity to pain's KEGG ID is recorded as H00774[11].
- congenital insensitivity to pain's MeSH tree code is recorded as C10.668.829.700[12].
- congenital insensitivity to pain's MeSH tree code is recorded as C16.320.775[13].
- congenital insensitivity to pain's health specialty is recorded as neurology[14].
- congenital insensitivity to pain's genetic association is recorded as SCN9A[15].
- congenital insensitivity to pain's Microsoft Academic ID is recorded as 2776054947[16].
- congenital insensitivity to pain's Genetics Home Reference Conditions ID is recorded as congenital-insensitivity-to-pain[17].
Why It Matters
congenital insensitivity to pain ranks in the top 7% of rare_disease entities by monthly Wikipedia readership (649 views/month).[2] It has Wikipedia articles in 16 language editions, a strong signal of global cultural recognition.[18] It is known by 8 alternative names across languages and contexts.[19]