holoprosencephaly 4
holoprosencephaly that has material basis in heterozygous mutation in the TGIF gene on chromosome 18p11
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holoprosencephaly 4
Summary
holoprosencephaly 4 is a rare disease[1].
Key Facts
- holoprosencephaly 4's instance of is recorded as rare disease[2].
- holoprosencephaly 4's instance of is recorded as class of disease[3].
- holoprosencephaly 4's subclass of is recorded as holoprosencephaly[4].
- holoprosencephaly 4's subclass of is recorded as genetic disease[5].
- holoprosencephaly 4's subclass of is recorded as autosomal dominant disease[6].
- holoprosencephaly 4's MeSH descriptor ID is recorded as C564180[7].
- holoprosencephaly 4's OMIM ID is recorded as 142946[8].
- holoprosencephaly 4's Disease Ontology ID is recorded as DOID:0110880[9].
- holoprosencephaly 4's NCI Thesaurus ID is recorded as C75475[10].
- holoprosencephaly 4's genetic association is recorded as TGIF1[11].
- holoprosencephaly 4's exact match is recorded as http://purl.obolibrary.org/obo/DOID_0110880[12].
- holoprosencephaly 4's exact match is recorded as http://identifiers.org/doid/DOID:0110880[13].
- holoprosencephaly 4's exact match is recorded as http://www.orpha.net/ORDO/Orphanet_2162[14].
- holoprosencephaly 4's UMLS CUI is recorded as C1840528[15].
- holoprosencephaly 4's on focus list of Wikimedia project is recorded as WikiProject Medicine[16].
- holoprosencephaly 4's Mondo ID is recorded as MONDO_0007734[17].
- holoprosencephaly 4's UniProt disease ID is recorded as DI-00568[18].