autosomal dominant Robinow syndrome 1
Human disease
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Summary
autosomal dominant Robinow syndrome 1 is a rare disease[1].
Key Facts
- autosomal dominant Robinow syndrome 1's instance of is recorded as rare disease[2].
- autosomal dominant Robinow syndrome 1's instance of is recorded as class of disease[3].
- autosomal dominant Robinow syndrome 1's subclass of is recorded as Robinow syndrome[4].
- autosomal dominant Robinow syndrome 1's subclass of is recorded as autosomal dominant disease[5].
- autosomal dominant Robinow syndrome 1's OMIM ID is recorded as 180700[6].
- autosomal dominant Robinow syndrome 1's Disease Ontology ID is recorded as DOID:0060766[7].
- autosomal dominant Robinow syndrome 1's Orphanet ID is recorded as 3107[8].
- autosomal dominant Robinow syndrome 1's Orphanet ID is recorded as 97360[9].
- autosomal dominant Robinow syndrome 1's genetic association is recorded as WNT5A[10].
- autosomal dominant Robinow syndrome 1's exact match is recorded as http://identifiers.org/doid/DOID:0060766[11].
- autosomal dominant Robinow syndrome 1's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0060766[12].
- autosomal dominant Robinow syndrome 1's UMLS CUI is recorded as C0265205[13].
- autosomal dominant Robinow syndrome 1's on focus list of Wikimedia project is recorded as WikiProject Medicine[14].
- autosomal dominant Robinow syndrome 1's Mondo ID is recorded as MONDO_0024455[15].
- autosomal dominant Robinow syndrome 1's UniProt disease ID is recorded as DI-03227[16].