Sotos syndrome
autosomal recessive disease that occurs rarely and is characterized by excessive physical growth during the first 2 to 3 years of life
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Sotos syndrome
Summary
Sotos syndrome is a developmental defect during embryogenesis[1]. It has Wikipedia articles in 14 language editions, a strong signal of global cultural recognition.[2]
Key Facts
- Sotos syndrome's instance of is recorded as developmental defect during embryogenesis[3].
- Sotos syndrome's instance of is recorded as rare disease[4].
- Sotos syndrome's instance of is recorded as class of disease[5].
- Sotos syndrome is a type of autosomal recessive disease[6].
- Sotos syndrome is a type of overgrowth syndrome[7].
- Sotos syndrome is a type of syndrome[8].
- Sotos syndrome is a type of autosomal genetic disease[9].
- Sotos syndrome is a type of disease[10].
- Sotos syndrome's Commons category is recorded as Sotos syndrome[11].
- Sotos syndrome's NCI Thesaurus ID is recorded as C75019[12].
- Sotos syndrome's health specialty is recorded as medical genetics[13].
- Sotos syndrome's genetic association is recorded as NSD1[14].
- Sotos syndrome's genetic association is recorded as NFIX[15].
- Sotos syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_14748[16].
- Sotos syndrome's exact match is recorded as http://identifiers.org/doid/DOID:14748[17].
- Sotos syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_821[18].
- Sotos syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
Why It Matters
Sotos 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.[20]