holoprosencephaly 5
holoprosencephaly that has material basis in heterozygous mutation in the ZIC2 gene on chromosome 13q32
Press Enter · cited answer in seconds
0 sources
holoprosencephaly 5
Summary
holoprosencephaly 5 is a class of disease[1]. It is known by 4 alternative names across languages and contexts.[2]
Key Facts
- holoprosencephaly 5's instance of is recorded as class of disease[3].
- holoprosencephaly 5 is a type of holoprosencephaly[4].
- holoprosencephaly 5 is a type of genetic disease[5].
- holoprosencephaly 5 is a type of autosomal dominant disease[6].
- holoprosencephaly 5's NCI Thesaurus ID is recorded as C75460[7].
- holoprosencephaly 5's genetic association is recorded as ZIC2[8].
- holoprosencephaly 5's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110878[9].
- holoprosencephaly 5's exact match is recorded as http://identifiers.org/doid/DOID:0110878[10].
- holoprosencephaly 5's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2162[11].
- holoprosencephaly 5's on focus list of Wikimedia project is recorded as WikiProject Medicine[12].
Why It Matters
holoprosencephaly 5 is known by 4 alternative names across languages and contexts.[2]