cone-rod dystrophy 2
cone-rod dystrophy that has material basis in heterozygous mutation in the CRX gene on chromosome 19q13
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cone-rod dystrophy 2
Summary
cone-rod dystrophy 2 is a rare disease[1].
Key Facts
- cone-rod dystrophy 2's instance of is recorded as rare disease[2].
- cone-rod dystrophy 2's instance of is recorded as class of disease[3].
- cone-rod dystrophy 2's subclass of is recorded as cone-rod dystrophy[4].
- cone-rod dystrophy 2's OMIM ID is recorded as 120970[5].
- cone-rod dystrophy 2's Disease Ontology ID is recorded as DOID:0111005[6].
- cone-rod dystrophy 2's ICD-9-CM is recorded as 362.75[7].
- cone-rod dystrophy 2's NCI Thesaurus ID is recorded as C162399[8].
- cone-rod dystrophy 2's genetic association is recorded as CRX[9].
- cone-rod dystrophy 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0111005[10].
- cone-rod dystrophy 2's exact match is recorded as http://identifiers.org/doid/DOID:0111005[11].
- cone-rod dystrophy 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_1872[12].
- cone-rod dystrophy 2's UMLS CUI is recorded as CN074280[13].
- cone-rod dystrophy 2's UMLS CUI is recorded as C0035334[14].
- cone-rod dystrophy 2's GARD rare disease ID is recorded as 6145[15].
- cone-rod dystrophy 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- cone-rod dystrophy 2's Mondo ID is recorded as MONDO_0007362[17].
- cone-rod dystrophy 2's UniProt disease ID is recorded as DI-00318[18].