Stickler syndrome type 1
human disease
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Stickler syndrome type 1
Summary
Stickler syndrome type 1 is a class of disease[1].
Key Facts
- Stickler syndrome type 1's instance of is recorded as class of disease[2].
- Stickler syndrome type 1's subclass of is recorded as Stickler syndrome[3].
- Stickler syndrome type 1's MeSH descriptor ID is recorded as C537492[4].
- Stickler syndrome type 1's OMIM ID is recorded as 108300[5].
- Stickler syndrome type 1's Orphanet ID is recorded as 90653[6].
- Stickler syndrome type 1's NCI Thesaurus ID is recorded as C168733[7].
- Stickler syndrome type 1's genetic association is recorded as COL2A1[8].
- Stickler syndrome type 1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_828[9].
- Stickler syndrome type 1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_90653[10].
- Stickler syndrome type 1's UMLS CUI is recorded as C2020284[11].
- Stickler syndrome type 1's ICD-10-CM is recorded as Q87.5[12].
- Stickler syndrome type 1's GARD rare disease ID is recorded as 5018[13].
- Stickler syndrome type 1's Mondo ID is recorded as MONDO_0007160[14].