Bardet-Biedl syndrome 15
Bardet-Biedl syndrome that has material basis in homozygous mutation in the WDPCP gene on chromosome 2p15
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Bardet-Biedl syndrome 15
Summary
Bardet-Biedl syndrome 15 is a rare disease[1].
Key Facts
- Bardet-Biedl syndrome 15's instance of is recorded as rare disease[2].
- Bardet-Biedl syndrome 15's instance of is recorded as class of disease[3].
- Bardet-Biedl syndrome 15's subclass of is recorded as Bardet-Biedl syndrome[4].
- Bardet-Biedl syndrome 15's OMIM ID is recorded as 615992[5].
- Bardet-Biedl syndrome 15's Disease Ontology ID is recorded as DOID:0110137[6].
- Bardet-Biedl syndrome 15's health specialty is recorded as medical genetics[7].
- Bardet-Biedl syndrome 15's genetic association is recorded as WDPCP[8].
- Bardet-Biedl syndrome 15's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110137[9].
- Bardet-Biedl syndrome 15's exact match is recorded as http://identifiers.org/doid/DOID:0110137[10].
- Bardet-Biedl syndrome 15's UMLS CUI is recorded as C3150127[11].
- Bardet-Biedl syndrome 15's ICD-10-CM is recorded as Q87.89[12].
- Bardet-Biedl syndrome 15's on focus list of Wikimedia project is recorded as WikiProject Medicine[13].
- Bardet-Biedl syndrome 15's Mondo ID is recorded as MONDO_0014443[14].
- Bardet-Biedl syndrome 15's UniProt disease ID is recorded as DI-02938[15].