Meier-Gorlin syndrome 8
human disease
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Meier-Gorlin syndrome 8
Summary
Meier-Gorlin syndrome 8 is a developmental defect during embryogenesis[1].
Key Facts
- Meier-Gorlin syndrome 8's instance of is recorded as developmental defect during embryogenesis[2].
- Meier-Gorlin syndrome 8's instance of is recorded as class of disease[3].
- Meier-Gorlin syndrome 8's subclass of is recorded as Meier-Gorlin syndrome[4].
- Meier-Gorlin syndrome 8's subclass of is recorded as autosomal recessive disease[5].
- Meier-Gorlin syndrome 8's OMIM ID is recorded as 617564[6].
- Meier-Gorlin syndrome 8's Disease Ontology ID is recorded as DOID:0080255[7].
- Meier-Gorlin syndrome 8's genetic association is recorded as MCM5[8].
- Meier-Gorlin syndrome 8's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0080255[9].
- Meier-Gorlin syndrome 8's exact match is recorded as http://identifiers.org/doid/DOID:0080255[10].
- Meier-Gorlin syndrome 8's UMLS CUI is recorded as C4479655[11].
- Meier-Gorlin syndrome 8's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
- Meier-Gorlin syndrome 8's Mondo ID is recorded as MONDO_0033046[13].
- Meier-Gorlin syndrome 8's UniProt disease ID is recorded as DI-05038[14].