Snyder-Robinson syndrome
Human disease
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Snyder-Robinson syndrome
Summary
Snyder-Robinson syndrome is a hereditary disorder[1]. It draws 105 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 is a type of X-linked intellectual disability[6].
- Snyder-Robinson syndrome is a type of X-linked recessive disease[7].
- Snyder-Robinson syndrome's ICD-9-CM is recorded as 758.89[8].
- Snyder-Robinson syndrome's health specialty is recorded as medical genetics[9].
- Snyder-Robinson syndrome's genetic association is recorded as SMS[10].
- Snyder-Robinson syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060802[11].
- Snyder-Robinson syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060802[12].
- Snyder-Robinson syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_3063[13].
- Snyder-Robinson syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
Why It Matters
Snyder-Robinson syndrome draws 105 Wikipedia views per month (hereditary_disorder category, ranking #7 of 25).[2]