Usher syndrome type 1
Usher syndrome characterized by profound congenital deafness, vestibular dysfunction and early development of retinitis pigmentosa
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Usher syndrome type 1
Summary
Usher syndrome type 1 is a class of disease[1].
Key Facts
- Usher syndrome type 1's instance of is recorded as class of disease[2].
- Usher syndrome type 1's subclass of is recorded as Usher syndrome[3].
- Usher syndrome type 1's OMIM ID is recorded as 276900[4].
- Usher syndrome type 1's Disease Ontology ID is recorded as DOID:0110826[5].
- Usher syndrome type 1's Orphanet ID is recorded as 231169[6].
- Usher syndrome type 1's NCI Thesaurus ID is recorded as C126327[7].
- Usher syndrome type 1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110826[8].
- Usher syndrome type 1's exact match is recorded as http://identifiers.org/doid/DOID:0110826[9].
- Usher syndrome type 1's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_231169[10].
- Usher syndrome type 1's UMLS CUI is recorded as C0339533[11].
- Usher syndrome type 1's ICD-10-CM is recorded as H35.5[12].
- Usher syndrome type 1's GARD rare disease ID is recorded as 5435[13].
- Usher syndrome type 1's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].