Apert syndrome
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Apert syndrome
Summary
Apert syndrome is a rare disease[1]. It draws 219 Wikipedia views per month (rare_disease category, ranking #104 of 627).[2]
Key Facts
- Apert syndrome's image is recorded as Patient with Apert syndrome.jpg[3].
- Apert syndrome's instance of is recorded as rare disease[4].
- Apert syndrome's instance of is recorded as class of disease[5].
- Apert syndrome's subclass of is recorded as acrocephalosyndactylia[6].
- Apert syndrome's Commons category is recorded as Apert syndrome[7].
- Apert syndrome's OMIM ID is recorded as 101200[8].
- Apert syndrome's ICD-9 ID is recorded as 755.55[9].
- Apert syndrome's ICD-10 ID is recorded as Q87.0[10].
- Apert syndrome's DiseasesDB is recorded as 33968[11].
- Apert syndrome's MedlinePlus ID is recorded as 001581[12].
- Apert syndrome's Freebase ID is recorded as /m/05768l[13].
- Apert syndrome's KEGG ID is recorded as H01755[14].
- Apert syndrome's ICPC 2 ID is recorded as A90[15].
- Apert syndrome's eMedicine ID is recorded as 941723[16].
- Apert syndrome's Orphanet ID is recorded as 87[17].
- Apert syndrome's NCI Thesaurus ID is recorded as C99099[18].
- Apert syndrome's health specialty is recorded as medical genetics[19].
- Apert syndrome's genetic association is recorded as FGFR2[20].
- Apert syndrome's Quora topic ID is recorded as Apert-Syndrome[21].
- Apert syndrome's WikiSkripta article ID is recorded as 3599[22].
- Apert syndrome's GARD rare disease ID is recorded as 5833[23].
- Apert syndrome's Store medisinske leksikon ID is recorded as akrocephalosyndactyli[24].
- Apert syndrome's Store medisinske leksikon ID is recorded as Aperts_syndrom[25].
- Apert syndrome's Mondo ID is recorded as MONDO_0007041[26].
- Apert syndrome's SNOMED CT ID is recorded as 205258009[27].
Why It Matters
Apert syndrome draws 219 Wikipedia views per month (rare_disease category, ranking #104 of 627).[2] It has Wikipedia articles in 16 language editions, a strong signal of global cultural recognition.[28] It is known by 16 alternative names across languages and contexts.[29]