Aarskog syndrome
monogenic disease affects a person's height, muscles, skeleton, genitals, and appearance of the face
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Summary
Aarskog syndrome is a rare disease[1]. It draws 323 Wikipedia views per month (rare_disease category, ranking #172 of 627).[2]
Key Facts
- Aarskog syndrome's instance of is recorded as rare disease[3].
- Aarskog syndrome's instance of is recorded as class of disease[4].
- Dagfinn Aarskog is named after Aarskog syndrome[5].
- Charles I. Scott is named after Aarskog syndrome[6].
- Aarskog syndrome is a type of malformation syndrome[7].
- Aarskog syndrome is a type of X-linked recessive disease[8].
- Aarskog syndrome is a type of X-linked intellectual disability[9].
- Aarskog syndrome is a type of syndrome[10].
- Aarskog syndrome's described at URL is recorded as https://rarediseases.org/rare-diseases/aarskog-syndrome/[11].
- Aarskog syndrome's mode of inheritance is recorded as X-linked recessive[12].
- Aarskog syndrome's ICD-9-CM is recorded as 759.89[13].
- Aarskog syndrome's NCI Thesaurus ID is recorded as C129720[14].
- Aarskog syndrome's health specialty is recorded as medical genetics[15].
- Aarskog syndrome's genetic association is recorded as FGD1[16].
- Aarskog syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111824[17].
- Aarskog syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0111824[18].
- Aarskog syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[19].
Why It Matters
Aarskog syndrome draws 323 Wikipedia views per month (rare_disease category, ranking #172 of 627).[2] It has Wikipedia articles in 17 language editions, a strong signal of global cultural recognition.[20] It is known by 69 alternative names across languages and contexts.[21]