MeSH Browser

MeSH Supplementary: cyclopia sequence
Unique ID: C562573
RDF Unique Identifier: http://id.nlm.nih.gov/mesh/C562573
Entry Term(s): Cyclopia; Cyclopia defect; Demyer Sequence; Holoprosencephaly 1; cyclocephaly; cyclopian defect; synophthalmia
Registry Number: 0
Heading Mapped to: *Holoprosencephaly
Frequency: 103
Note: A hereditary autosomal recessive form of holoprosencephaly which maps to chromosome 21. OMIM: 236100
Date of Entry: 2012/11/05
Revision Date: 2020/09/30

Concept UI: M0562873
Registry Number: 0
Terms: cyclopia sequence Preferred Term
Term UI T000994641
Date10/21/2019
LexicalTag NON
ThesaurusID NLM (2020); Holoprosencephaly 1
Term UI T806911
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Cyclopia defect
Term UI T000994640
Date10/21/2019
LexicalTag NON
ThesaurusID NLM (2020); cyclocephaly
Term UI T000994636
Date10/21/2019
LexicalTag NON
ThesaurusID NLM (2020); synophthalmia
Term UI T000994637
Date10/21/2019
LexicalTag NON
ThesaurusID NLM (2020); cyclopian defect
Term UI T000994639
Date10/21/2019
LexicalTag NON
ThesaurusID NLM (2020); Cyclopia
Term UI T800962
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013); Demyer Sequence
Term UI T810759
Date11/15/2011
LexicalTag NON
ThesaurusID OMIM (2013)

cyclopia sequence MeSH Supplementary Concept Data 2024