Meier-Gorlin syndrome 7; MGORS7
human disease
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Meier-Gorlin syndrome 7; MGORS7
Summary
Meier-Gorlin syndrome 7; MGORS7 is a developmental defect during embryogenesis[1].
Key Facts
- Meier-Gorlin syndrome 7; MGORS7's instance of is recorded as developmental defect during embryogenesis[2].
- Meier-Gorlin syndrome 7; MGORS7's instance of is recorded as rare disease[3].
- Meier-Gorlin syndrome 7; MGORS7's instance of is recorded as disease[4].
- Meier-Gorlin syndrome 7; MGORS7's instance of is recorded as class of disease[5].
- Meier-Gorlin syndrome 7; MGORS7's subclass of is recorded as Meier-Gorlin syndrome[6].
- Meier-Gorlin syndrome 7; MGORS7's subclass of is recorded as autosomal recessive disease[7].
- Meier-Gorlin syndrome 7; MGORS7's OMIM ID is recorded as 617063[8].
- Meier-Gorlin syndrome 7; MGORS7's Disease Ontology ID is recorded as DOID:0080518[9].
- Meier-Gorlin syndrome 7; MGORS7's genetic association is recorded as CDC45[10].
- Meier-Gorlin syndrome 7; MGORS7's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080518[11].
- Meier-Gorlin syndrome 7; MGORS7's exact match is recorded as http://identifiers.org/doid/DOID:0080518[12].
- Meier-Gorlin syndrome 7; MGORS7's UMLS CUI is recorded as C4310738[13].
- Meier-Gorlin syndrome 7; MGORS7's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- Meier-Gorlin syndrome 7; MGORS7's Mondo ID is recorded as MONDO_0014894[15].
- Meier-Gorlin syndrome 7; MGORS7's UniProt disease ID is recorded as DI-04797[16].