Parry–Romberg syndrome
a rare disease characterized by progressive shrinkage and degeneration of the tissues beneath the skin, usually on only one side of the face (hemifacial atrophy) but occasionally extending to other parts of the body
Press Enter · cited answer in seconds
0 sources
Parry–Romberg syndrome
Summary
Parry–Romberg syndrome is a class of disease[1]. It draws 133 Wikipedia views per month (class_of_disease category, ranking #500 of 1,968).[2]
Key Facts
- Parry–Romberg syndrome's image is recorded as Parry Romberg Syndrome 1.jpg[3].
- Parry–Romberg syndrome's instance of is recorded as class of disease[4].
- Moritz Heinrich Romberg is named after Parry–Romberg syndrome[5].
- Caleb Hillier Parry is named after Parry–Romberg syndrome[6].
- Parry–Romberg syndrome's subclass of is recorded as facial nerve disease[7].
- Parry–Romberg syndrome's subclass of is recorded as brain inflammatory disease[8].
- Parry–Romberg syndrome's subclass of is recorded as inflammatory and autoimmune disease with epilepsy[9].
- Parry–Romberg syndrome's subclass of is recorded as genetic peripheral neuropathy[10].
- Parry–Romberg syndrome's subclass of is recorded as rare genetic epilepsy[11].
- Parry–Romberg syndrome's subclass of is recorded as disease[12].
- Parry–Romberg syndrome's Commons category is recorded as Parry–Romberg syndrome[13].
- Parry–Romberg syndrome's MeSH descriptor ID is recorded as D005150[14].
- Parry–Romberg syndrome's OMIM ID is recorded as 141300[15].
- Parry–Romberg syndrome's ICD-9 ID is recorded as 349.89[16].
- Parry–Romberg syndrome's ICD-9 ID is recorded as 351.8[17].
- Parry–Romberg syndrome's ICD-10 ID is recorded as G51.8[18].
- Parry–Romberg syndrome's DiseasesDB is recorded as 30151[19].
- Parry–Romberg syndrome's Freebase ID is recorded as /m/026d6m7[20].
- Parry–Romberg syndrome's MeSH tree code is recorded as C07.465.284[21].
- Parry–Romberg syndrome's MeSH tree code is recorded as C07.465.299.375[22].
- Parry–Romberg syndrome's MeSH tree code is recorded as C10.292.319.375[23].
- Parry–Romberg syndrome's Disease Ontology ID is recorded as DOID:1757[24].
- Parry–Romberg syndrome's Orphanet ID is recorded as 1214[25].
- Parry–Romberg syndrome's NCI Thesaurus ID is recorded as C84703[26].
- Parry–Romberg syndrome's NCI Thesaurus ID is recorded as C116916[27].
Why It Matters
Parry–Romberg syndrome draws 133 Wikipedia views per month (class_of_disease category, ranking #500 of 1,968).[2] It has Wikipedia articles in 12 language editions, a strong signal of global cultural recognition.[28] It is known by 10 alternative names across languages and contexts.[29]