Kallmann syndrome
form of hypogonadotropic hypogonadism which is also accompanied by a total lack or partial loss in the sense of smell. The condition affects people with XX or XY chromosomes and causes atypical puberty and infertility
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Kallmann syndrome
Summary
Kallmann syndrome is a class of disease[1]. It draws 1,441 Wikipedia views per month (class_of_disease category, ranking #256 of 1,968).[2]
Key Facts
- Kallmann syndrome's instance of is recorded as class of disease[3].
- Franz Josef Kallmann is named after Kallmann syndrome[4].
- Kallmann syndrome is a type of hypogonadotropic hypogonadism[5].
- Kallmann syndrome is a type of disease[6].
- Kallmann syndrome is a type of intersex variation[7].
- Kallmann syndrome's Commons category is recorded as Kallmann syndrome[8].
- Kallmann syndrome's symptoms and signs is recorded as anosmia[9].
- Kallmann syndrome's symptoms and signs is recorded as hypogonadism[10].
- Kallmann syndrome's symptoms and signs is recorded as osteoporosis[11].
- Kallmann syndrome's symptoms and signs is recorded as infertility[12].
- Kallmann syndrome's NCI Thesaurus ID is recorded as C75479[13].
- Kallmann syndrome's health specialty is recorded as endocrinology[14].
- Kallmann syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_3614[15].
- Kallmann syndrome's exact match is recorded as http://identifiers.org/doid/DOID:3614[16].
- Kallmann syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_478[17].
- Kallmann syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[18].
Why It Matters
Kallmann syndrome draws 1,441 Wikipedia views per month (class_of_disease category, ranking #256 of 1,968).[2] It has Wikipedia articles in 20 language editions, a strong signal of global cultural recognition.[19] It is known by 34 alternative names across languages and contexts.[20]