holoprosencephaly 2
holoprosencephaly that has material basis in mutation in the homeobox-containing SIX3 gene on chromosome 2p21
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holoprosencephaly 2
Summary
holoprosencephaly 2 is a class of disease[1].
Key Facts
- holoprosencephaly 2's instance of is recorded as class of disease[2].
- holoprosencephaly 2's subclass of is recorded as holoprosencephaly[3].
- holoprosencephaly 2's subclass of is recorded as genetic disease[4].
- holoprosencephaly 2's subclass of is recorded as autosomal dominant disease[5].
- holoprosencephaly 2's MeSH descriptor ID is recorded as C563579[6].
- holoprosencephaly 2's OMIM ID is recorded as 157170[7].
- holoprosencephaly 2's Disease Ontology ID is recorded as DOID:0110872[8].
- holoprosencephaly 2's NCI Thesaurus ID is recorded as C74995[9].
- holoprosencephaly 2's genetic association is recorded as SIX3[10].
- holoprosencephaly 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110872[11].
- holoprosencephaly 2's exact match is recorded as http://identifiers.org/doid/DOID:0110872[12].
- holoprosencephaly 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2162[13].
- holoprosencephaly 2's UMLS CUI is recorded as C1834877[14].
- holoprosencephaly 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- holoprosencephaly 2's Mondo ID is recorded as MONDO_0007999[16].
- holoprosencephaly 2's UniProt disease ID is recorded as DI-00566[17].