Netherton syndrome
Human disease
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Netherton syndrome
Summary
Netherton syndrome is a rare disease[1]. It has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Netherton syndrome's instance of is recorded as rare disease[3].
- Netherton syndrome's instance of is recorded as class of disease[4].
- Netherton syndrome is a type of autosomal recessive disease[5].
- Netherton syndrome is a type of ichthyosis[6].
- Netherton syndrome is a type of skin disease[7].
- Netherton syndrome's symptoms and signs is recorded as Trichorrhexis invaginata[8].
- Netherton syndrome's symptoms and signs is recorded as inflammation[9].
- Netherton syndrome's NCI Thesaurus ID is recorded as C84922[10].
- Netherton syndrome's health specialty is recorded as medical genetics[11].
- Netherton syndrome's genetic association is recorded as SPINK5[12].
- Netherton syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0050474[13].
- Netherton syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0050474[14].
- Netherton syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_634[15].
- Netherton syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
Why It Matters
Netherton syndrome has Wikipedia articles in 7 language editions, a strong signal of global cultural recognition.[2] It is known by 11 alternative names across languages and contexts.[17]