Wolf-Hirschhorn syndrome
chromosome abnormality with a distinct craniofacial phenotype and intellectual disability
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Wolf-Hirschhorn syndrome
Summary
Wolf-Hirschhorn syndrome is a class of disease[1]. It has Wikipedia articles in 14 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Wolf-Hirschhorn syndrome's instance of is recorded as class of disease[3].
- Kurt Hirschhorn is named after Wolf-Hirschhorn syndrome[4].
- Ulrich Wolf is named after Wolf-Hirschhorn syndrome[5].
- Wolf-Hirschhorn syndrome is a type of chromosomal deletion syndrome[6].
- Wolf-Hirschhorn syndrome is a type of partial deletion of the short arm of chromosome 4[7].
- Wolf-Hirschhorn syndrome is a type of disease[8].
- Wolf-Hirschhorn syndrome's Commons category is recorded as Wolf–Hirschhorn syndrome[9].
- Wolf-Hirschhorn syndrome's NCI Thesaurus ID is recorded as C35528[10].
- Wolf-Hirschhorn syndrome's health specialty is recorded as medical genetics[11].
- Wolf-Hirschhorn syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050460[12].
- Wolf-Hirschhorn syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050460[13].
- Wolf-Hirschhorn syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
Wolf-Hirschhorn syndrome has Wikipedia articles in 14 language editions, a strong signal of global cultural recognition.[2] It is known by 14 alternative names across languages and contexts.[15]