Warburg micro syndrome 4
Warburg micro syndrome that has material basis in autosomal recessive inheritance of homozygous or compound heterozygous mutation in the TBC1D20 gene on chromosome 20p13
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Warburg micro syndrome 4
Summary
Warburg micro syndrome 4 is a rare disease[1].
Key Facts
- Warburg micro syndrome 4's instance of is recorded as rare disease[2].
- Warburg micro syndrome 4's instance of is recorded as class of disease[3].
- Warburg micro syndrome 4's subclass of is recorded as Warburg micro syndrome[4].
- Warburg micro syndrome 4's OMIM ID is recorded as 615663[5].
- Warburg micro syndrome 4's OMIM ID is recorded as 615663[6].
- Warburg micro syndrome 4's Disease Ontology ID is recorded as DOID:0110719[7].
- Warburg micro syndrome 4's health specialty is recorded as medical genetics[8].
- Warburg micro syndrome 4's genetic association is recorded as TBC1D20[9].
- Warburg micro syndrome 4's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110719[10].
- Warburg micro syndrome 4's exact match is recorded as http://identifiers.org/doid/DOID:0110719[11].
- Warburg micro syndrome 4's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2510[12].
- Warburg micro syndrome 4's UMLS CUI is recorded as C3810265[13].
- Warburg micro syndrome 4's ICD-10-CM is recorded as Q87.0[14].
- Warburg micro syndrome 4's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- Warburg micro syndrome 4's Mondo ID is recorded as MONDO_0014296[16].
- Warburg micro syndrome 4's UniProt disease ID is recorded as DI-04041[17].