Alwadei syndrome
autosomal recessive non-syndromic intellectual disability that has material basis in an autosomal recessive mutation of the RUSC2 gene on chromosome 9p13
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Alwadei syndrome
Summary
Alwadei syndrome is a class of disease[1]. It draws 1 Wikipedia views per month (class_of_disease category, ranking #631 of 1,968).[2]
Key Facts
- Alwadei syndrome's instance of is recorded as class of disease[3].
- Alwadei syndrome's subclass of is recorded as autosomal recessive non-syndromic intellectual disability[4].
- Alwadei syndrome's subclass of is recorded as neurodevelopmental disorder[5].
- Alwadei syndrome's OMIM ID is recorded as 617773[6].
- Alwadei syndrome's Disease Ontology ID is recorded as DOID:0080239[7].
- Alwadei syndrome's health specialty is recorded as neurology[8].
- Alwadei syndrome's genetic association is recorded as RUSC2[9].
- Alwadei syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080239[10].
- Alwadei syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0080239[11].
- Alwadei syndrome's UMLS CUI is recorded as C4540424[12].
- Alwadei syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- Alwadei syndrome's Mondo ID is recorded as MONDO_0030915[14].
- Alwadei syndrome's UniProt disease ID is recorded as DI-05133[15].
Why It Matters
Alwadei syndrome draws 1 Wikipedia views per month (class_of_disease category, ranking #631 of 1,968).[2]