holoprosencephaly 7
holoprosencephaly that has material basis in heterozygous mutation in the PTCH1 gene on chromosome 9q22
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holoprosencephaly 7
Summary
holoprosencephaly 7 is a rare disease[1].
Key Facts
- holoprosencephaly 7's instance of is recorded as rare disease[2].
- holoprosencephaly 7's instance of is recorded as class of disease[3].
- holoprosencephaly 7's subclass of is recorded as holoprosencephaly[4].
- holoprosencephaly 7's subclass of is recorded as genetic disease[5].
- holoprosencephaly 7's MeSH descriptor ID is recorded as C563660[6].
- holoprosencephaly 7's OMIM ID is recorded as 610828[7].
- holoprosencephaly 7's OMIM ID is recorded as 610828[8].
- holoprosencephaly 7's Disease Ontology ID is recorded as DOID:0110876[9].
- holoprosencephaly 7's genetic association is recorded as PTCH1[10].
- holoprosencephaly 7's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110876[11].
- holoprosencephaly 7's exact match is recorded as http://identifiers.org/doid/DOID:0110876[12].
- holoprosencephaly 7's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2162[13].
- holoprosencephaly 7's UMLS CUI is recorded as C1835820[14].
- holoprosencephaly 7's on focus list of Wikimedia project is recorded as WikiProject Medicine[15].
- holoprosencephaly 7's Mondo ID is recorded as MONDO_0012562[16].
- holoprosencephaly 7's UniProt disease ID is recorded as DI-00570[17].