Warburg micro syndrome 2
Warburg micro syndrome that has material basis in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB3GAP2 gene on chromosome 1q41
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Warburg micro syndrome 2
Summary
Warburg micro syndrome 2 is a rare disease[1].
Key Facts
- Warburg micro syndrome 2's instance of is recorded as rare disease[2].
- Warburg micro syndrome 2's instance of is recorded as class of disease[3].
- Warburg micro syndrome 2's subclass of is recorded as Warburg micro syndrome[4].
- Warburg micro syndrome 2's OMIM ID is recorded as 614225[5].
- Warburg micro syndrome 2's OMIM ID is recorded as 614225[6].
- Warburg micro syndrome 2's Disease Ontology ID is recorded as DOID:0110717[7].
- Warburg micro syndrome 2's health specialty is recorded as medical genetics[8].
- Warburg micro syndrome 2's genetic association is recorded as RAB3GAP2[9].
- Warburg micro syndrome 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110717[10].
- Warburg micro syndrome 2's exact match is recorded as http://identifiers.org/doid/DOID:0110717[11].
- Warburg micro syndrome 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2510[12].
- Warburg micro syndrome 2's UMLS CUI is recorded as C3280214[13].
- Warburg micro syndrome 2's ICD-10-CM is recorded as Q87.0[14].
- Warburg micro syndrome 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- Warburg micro syndrome 2's Mondo ID is recorded as MONDO_0013641[16].
- Warburg micro syndrome 2's UniProt disease ID is recorded as DI-03228[17].