Snyder-Robinson syndrome
Human disease
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Snyder-Robinson syndrome
Summary
Snyder-Robinson syndrome is a hereditary disorder[1]. It draws 20 Wikipedia views per month (hereditary_disorder category, ranking #7 of 25).[2]
Key Facts
- Snyder-Robinson syndrome's instance of is recorded as hereditary disorder[3].
- Snyder-Robinson syndrome's instance of is recorded as rare disease[4].
- Snyder-Robinson syndrome's instance of is recorded as class of disease[5].
- Snyder-Robinson syndrome's subclass of is recorded as X-linked intellectual disability[6].
- Snyder-Robinson syndrome's subclass of is recorded as X-linked recessive disease[7].
- Snyder-Robinson syndrome's MeSH descriptor ID is recorded as C536678[8].
- Snyder-Robinson syndrome's OMIM ID is recorded as 309583[9].
- Snyder-Robinson syndrome's DiseasesDB is recorded as 35186[10].
- Snyder-Robinson syndrome's KEGG ID is recorded as H00597[11].
- Snyder-Robinson syndrome's Disease Ontology ID is recorded as DOID:0060802[12].
- Snyder-Robinson syndrome's Orphanet ID is recorded as 3063[13].
- Snyder-Robinson syndrome's ICD-9-CM is recorded as 758.89[14].
- Snyder-Robinson syndrome's health specialty is recorded as medical genetics[15].
- Snyder-Robinson syndrome's genetic association is recorded as SMS[16].
- Snyder-Robinson syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060802[17].
- Snyder-Robinson syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060802[18].
- Snyder-Robinson syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3063[19].
- Snyder-Robinson syndrome's UMLS CUI is recorded as C0796160[20].
- Snyder-Robinson syndrome's ICD-10-CM is recorded as Q87.8[21].
- Snyder-Robinson syndrome's GARD rare disease ID is recorded as 5615[22].
- Snyder-Robinson syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[23].
- Snyder-Robinson syndrome's Mondo ID is recorded as MONDO_0010664[24].
- Snyder-Robinson syndrome's SNOMED CT ID is recorded as 702416008[25].
- Snyder-Robinson syndrome's WikiProjectMed ID is recorded as Snyder–Robinson syndrome[26].
- Snyder-Robinson syndrome's UniProt disease ID is recorded as DI-02315[27].
Why It Matters
Snyder-Robinson syndrome draws 20 Wikipedia views per month (hereditary_disorder category, ranking #7 of 25).[2]