Warburg micro syndrome
autosomal recessive disease characterized by severe intellectual disability, microcephaly, congenital cataract, microcornea, microphthalmia, agenesis or hypoplasia of the corpus callosum and hypogenitalism
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Warburg micro syndrome
Summary
Warburg micro syndrome is a rare disease[1].
Key Facts
- Warburg micro syndrome's instance of is recorded as rare disease[2].
- Warburg micro syndrome's instance of is recorded as class of disease[3].
- Mette Warburg is named after Warburg micro syndrome[4].
- Warburg micro syndrome's subclass of is recorded as autosomal recessive disease[5].
- Warburg micro syndrome's subclass of is recorded as syndrome[6].
- Warburg micro syndrome's MeSH descriptor ID is recorded as C536681[7].
- Warburg micro syndrome's OMIM ID is recorded as 600118[8].
- Warburg micro syndrome's KEGG ID is recorded as H00792[9].
- Warburg micro syndrome's Disease Ontology ID is recorded as DOID:0060237[10].
- Warburg micro syndrome's Orphanet ID is recorded as 2510[11].
- Warburg micro syndrome's genetic association is recorded as RAB3GAP1[12].
- Warburg micro syndrome's genetic association is recorded as RAB18[13].
- Warburg micro syndrome's genetic association is recorded as RAB3GAP2[14].
- Warburg micro syndrome's genetic association is recorded as TBC1D20[15].
- Warburg micro syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060237[16].
- Warburg micro syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060237[17].
- Warburg micro syndrome's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2510[18].
- Warburg micro syndrome's UMLS CUI is recorded as C1838625[19].
- Warburg micro syndrome's GARD rare disease ID is recorded as 5534[20].
- Warburg micro syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[21].
- Warburg micro syndrome's Microsoft Academic ID is recorded as 2780565095[22].
- Warburg micro syndrome's WikiProjectMed ID is recorded as Warburg Micro syndrome[23].