autosomal recessive Robinow syndrome
Human disease
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autosomal recessive Robinow syndrome
Summary
autosomal recessive Robinow syndrome is a class of disease[1].
Key Facts
- autosomal recessive Robinow syndrome's instance of is recorded as class of disease[2].
- autosomal recessive Robinow syndrome's subclass of is recorded as Robinow syndrome[3].
- autosomal recessive Robinow syndrome's subclass of is recorded as autosomal recessive disease[4].
- autosomal recessive Robinow syndrome's MeSH descriptor ID is recorded as C535863[5].
- autosomal recessive Robinow syndrome's OMIM ID is recorded as 268310[6].
- autosomal recessive Robinow syndrome's Disease Ontology ID is recorded as DOID:0060764[7].
- autosomal recessive Robinow syndrome's Orphanet ID is recorded as 1507[8].
- autosomal recessive Robinow syndrome's genetic association is recorded as ROR2[9].
- autosomal recessive Robinow syndrome's exact match is recorded as http://identifiers.org/doid/DOID:0060764[10].
- autosomal recessive Robinow syndrome's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060764[11].
- autosomal recessive Robinow syndrome's UMLS CUI is recorded as C1849334[12].
- autosomal recessive Robinow syndrome's UMLS CUI is recorded as C3151609[13].
- autosomal recessive Robinow syndrome's UMLS CUI is recorded as C3151610[14].
- autosomal recessive Robinow syndrome's ICD-10-CM is recorded as Q87.1[15].
- autosomal recessive Robinow syndrome's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- autosomal recessive Robinow syndrome's Mondo ID is recorded as MONDO_0009999[17].
- autosomal recessive Robinow syndrome's UniProt disease ID is recorded as DI-02247[18].