01
ABCA4
No data
- Entity Type
- Diseases
- Relation Groups
- 3
- Relation Preview
- 24
Basic Information
Grouped by core information, identifiers, and descriptions.
Current candidates are inferred from disease-target-ingredient-herb paths and do not represent a formal recommendation ranking.
Core Information
- Disease Name
- Cleft Lip
- Standard Disease Name
- cleft lip
- MeSH Tree
- No data
- ICD-10
- Q36|Q36.9
Identifiers
- DO ID
- No data
- MeSH ID
- D002971
- OMIM ID
- MTHU036343
- UMLS ID
- C0008924
- HPO ID
- No data
Description and Extensions
- Description
- NCI2016_CDISC_1602D:Fissure or split of the upper lip. (Makris S, Solomon HM, Clark R, Shiota K, Barbellion S, Buschmann J, Ema M, Fujiwara M, Grote K, Hazelden KP, Hew KW, Horimoto M, Ooshima Y, Parkinson M, Wise LD. Terminology of developmental abnormalities in common laboratory mammals (Version 2). Part B. Birth Defects Res B Dev Reprod Toxicol. 2009 Aug;86(4):227-327.)|NCI2016_02D:A congenital abnormality consisting of one or more clefts (splits) in the upper lip, which may be accompanied by a cleft palate; it is the result of the failure of the embryonic parts of the lip to fuse.|MSH2017_2016_08_12:Congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences. It is thought to be caused by faulty migration of the mesoderm in the head region.|HPO2016_07_04:A gap in the upper lip. This is a congenital defect resulting from nonfusion of tissues of the lip during embryonal development. [HPO:probinson]|CSP2006:congenital defect in the upper lip where the maxillary prominence fails to merge with the merged medial nasal prominences; thought to be caused by faulty migration of the mesoderm in the head region.