Warburg micro syndrome 3
Warburg micro syndrome that has material basis in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the RAB18 gene on chromosome 10p12
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Warburg micro syndrome 3
Summary
Warburg micro syndrome 3 is a rare disease[1].
Key Facts
- Warburg micro syndrome 3's instance of is recorded as rare disease[2].
- Warburg micro syndrome 3's instance of is recorded as class of disease[3].
- Warburg micro syndrome 3's subclass of is recorded as Warburg micro syndrome[4].
- Warburg micro syndrome 3's OMIM ID is recorded as 614222[5].
- Warburg micro syndrome 3's OMIM ID is recorded as 614222[6].
- Warburg micro syndrome 3's Disease Ontology ID is recorded as DOID:0110718[7].
- Warburg micro syndrome 3's health specialty is recorded as medical genetics[8].
- Warburg micro syndrome 3's genetic association is recorded as RAB18[9].
- Warburg micro syndrome 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110718[10].
- Warburg micro syndrome 3's exact match is recorded as http://identifiers.org/doid/DOID:0110718[11].
- Warburg micro syndrome 3's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2510[12].
- Warburg micro syndrome 3's UMLS CUI is recorded as C3280203[13].
- Warburg micro syndrome 3's ICD-10-CM is recorded as Q87.0[14].
- Warburg micro syndrome 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- Warburg micro syndrome 3's Mondo ID is recorded as MONDO_0013638[16].
- Warburg micro syndrome 3's UniProt disease ID is recorded as DI-03229[17].