Parkes Weber syndrome
uncommon congenital vascular malformation (CVM) characterized by the venous malformations, cutaneous capillary malformations, and lymphatic malformations along with arteriovenous malformation.
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Parkes Weber syndrome
Summary
Parkes Weber syndrome is a class of disease[1]. It draws 27 Wikipedia views per month (class_of_disease category, ranking #610 of 1,968).[2]
Key Facts
- Parkes Weber syndrome's instance of is recorded as class of disease[3].
- Frederick Parkes Weber is named after Parkes Weber syndrome[4].
- Parkes Weber syndrome's subclass of is recorded as Klippel–Trénaunay–Weber syndrome[5].
- Parkes Weber syndrome's OMIM ID is recorded as 608355[6].
- Parkes Weber syndrome's ICD-9 ID is recorded as 759.6[7].
- Parkes Weber syndrome's DiseasesDB is recorded as 33714[8].
- Parkes Weber syndrome's KEGG ID is recorded as H00532[9].
- Parkes Weber syndrome's Orphanet ID is recorded as 90307[10].
- Parkes Weber syndrome's different from is recorded as Klippel–Trénaunay–Weber syndrome[11].
- Parkes Weber syndrome's health specialty is recorded as medical genetics[12].
- Parkes Weber syndrome's PatientsLikeMe condition ID is recorded as parkes-weber-syndrome[13].
- Parkes Weber syndrome's GARD rare disease ID is recorded as 9787[14].
- Parkes Weber syndrome's Microsoft Academic ID is recorded as 2776424344[15].
- Parkes Weber syndrome's Genetics Home Reference Conditions ID is recorded as parkes-weber-syndrome[16].
- Parkes Weber syndrome's ICD-11 ID is recorded as 1412478956[17].
- Parkes Weber syndrome's WikiProjectMed ID is recorded as Parkes Weber syndrome[18].
Why It Matters
Parkes Weber syndrome draws 27 Wikipedia views per month (class_of_disease category, ranking #610 of 1,968).[2] It has Wikipedia articles in 5 language editions, a strong signal of global cultural recognition.[19]