holoprosencephaly 3
holoprosencephaly that has material basis in heterozygous mutation in the SHH gene on chromosome 7q36
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holoprosencephaly 3
Summary
holoprosencephaly 3 is a rare disease[1].
Key Facts
- holoprosencephaly 3's instance of is recorded as rare disease[2].
- holoprosencephaly 3's instance of is recorded as class of disease[3].
- holoprosencephaly 3's subclass of is recorded as holoprosencephaly[4].
- holoprosencephaly 3's subclass of is recorded as genetic disease[5].
- holoprosencephaly 3's subclass of is recorded as autosomal dominant disease[6].
- holoprosencephaly 3's MeSH descriptor ID is recorded as C564181[7].
- holoprosencephaly 3's OMIM ID is recorded as 142945[8].
- holoprosencephaly 3's Disease Ontology ID is recorded as DOID:0110875[9].
- holoprosencephaly 3's genetic association is recorded as SHH[10].
- holoprosencephaly 3's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110875[11].
- holoprosencephaly 3's exact match is recorded as http://identifiers.org/doid/DOID:0110875[12].
- holoprosencephaly 3's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2162[13].
- holoprosencephaly 3's UMLS CUI is recorded as C1840529[14].
- holoprosencephaly 3's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- holoprosencephaly 3's Mondo ID is recorded as MONDO_0007733[16].
- holoprosencephaly 3's UniProt disease ID is recorded as DI-00567[17].