autosomal dominant Robinow syndrome 3
Human disease
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Summary
autosomal dominant Robinow syndrome 3 is a rare disease[1].
Key Facts
- autosomal dominant Robinow syndrome 3's instance of is recorded as rare disease[2].
- autosomal dominant Robinow syndrome 3's instance of is recorded as class of disease[3].
- autosomal dominant Robinow syndrome 3's subclass of is recorded as Robinow syndrome[4].
- autosomal dominant Robinow syndrome 3's subclass of is recorded as autosomal dominant disease[5].
- autosomal dominant Robinow syndrome 3's OMIM ID is recorded as 616894[6].
- autosomal dominant Robinow syndrome 3's Disease Ontology ID is recorded as DOID:0060767[7].
- autosomal dominant Robinow syndrome 3's Orphanet ID is recorded as 3107[8].
- autosomal dominant Robinow syndrome 3's Orphanet ID is recorded as 97360[9].
- autosomal dominant Robinow syndrome 3's genetic association is recorded as DVL3[10].
- autosomal dominant Robinow syndrome 3's exact match is recorded as http://identifiers.org/doid/DOID:0060767[11].
- autosomal dominant Robinow syndrome 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060767[12].
- autosomal dominant Robinow syndrome 3's UMLS CUI is recorded as C4225164[13].
- autosomal dominant Robinow syndrome 3's ICD-10-CM is recorded as Alexandria.1[14].
- autosomal dominant Robinow syndrome 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- autosomal dominant Robinow syndrome 3's Mondo ID is recorded as MONDO_0014819[16].
- autosomal dominant Robinow syndrome 3's UniProt disease ID is recorded as DI-04701[17].