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 is a type of holoprosencephaly[3].
- holoprosencephaly 2 is a type of genetic disease[4].
- holoprosencephaly 2 is a type of autosomal dominant disease[5].
- holoprosencephaly 2's NCI Thesaurus ID is recorded as C74995[6].
- holoprosencephaly 2's genetic association is recorded as SIX3[7].
- holoprosencephaly 2's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110872[8].
- holoprosencephaly 2's exact match is recorded as http://identifiers.org/doid/DOID:0110872[9].
- holoprosencephaly 2's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2162[10].
- holoprosencephaly 2's on focus list of Wikimedia project is recorded as WikiProject Medicine[11].