Orofacial cleft 2

Preferred Label : Orofacial cleft 2;

Symbol : OFC2;

CISMeF acronym : OFC2;

Type : Phenotype or locus, molecular basis unknown;

Alternative titles and symbols : Cleft lip with or without cleft palate, nonsyndromic, 2;

Description : For a phenotypic description and a discussion of genetic heterogeneity of nonsyndromic cleft lip/palate (CL/P), see 119530.;

Inheritance : Autosomal dominant;

Prefixed ID : %602966;

Details

Origin ID

602966;

UMLS CUI

C1864323;

Automatic exact mappings (from CISMeF team)
- Cleft lip with or without cleft palate [ORDO Disease]
- TFAP2B Gene [NCIt concept]
- Transcription Factor AP-2-Beta [NCIt concept]
- orofacial cleft 2 [DO Concept]
- orofacial cleft 2 [HGNC gene]
Currated CISMeF NLP mapping
- orofacial cleft 2 [MeSH concept]
- orofacial cleft 2 [MeSH Supplementary Concept]
DO Cross reference
- orofacial cleft 2 [DO Concept]
ORDO concept(s)
- Cleft lip and alveolus [ORDO Disease]
- Cleft lip/palate [ORDO Disease]
- Isolated cleft lip [ORDO Disease]
Semantic type(s)
- Disease or Syndrome [UMLS semantic type]
UMLS correspondences (same concept)
- orofacial cleft 2 [MeSH Supplementary Concept]
- orofacial cleft 2 [MeSH concept]

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