Pelger-Huet anomaly
human disease
Press Enter · cited answer in seconds
0 sources
Pelger-Huet anomaly
Summary
Pelger-Huet anomaly is a rare disease[1]. It draws 196 Wikipedia views per month (rare_disease category, ranking #209 of 627).[2]
Key Facts
- Pelger-Huet anomaly's instance of is recorded as rare disease[3].
- Pelger-Huet anomaly's instance of is recorded as class of disease[4].
- Pelger-Huet anomaly is a type of leukocyte disease[5].
- Pelger-Huet anomaly is a type of autosomal dominant disease[6].
- Pelger-Huet anomaly is a type of hematopoietic system disease[7].
- Pelger-Huet anomaly's NCI Thesaurus ID is recorded as C85002[8].
- Pelger-Huet anomaly's health specialty is recorded as hematology[9].
- Pelger-Huet anomaly's genetic association is recorded as LBR[10].
- Pelger-Huet anomaly's exact match is recorded as http://purl.obolibrary.org/obo/DOID_9631[11].
- Pelger-Huet anomaly's exact match is recorded as http://identifiers.org/doid/DOID:9631[12].
- Pelger-Huet anomaly's exact match is recorded as http://purl.obolibrary.org/obo/HP_0011447[13].
- Pelger-Huet anomaly's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
Pelger-Huet anomaly draws 196 Wikipedia views per month (rare_disease category, ranking #209 of 627).[2] It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[15] It is known by 6 alternative names across languages and contexts.[16]