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Medical Subject Headings
Last uploaded:
March 22, 2026
| Id | http://purl.bioontology.org/ontology/MESH/C408373
http://purl.bioontology.org/ontology/MESH/C408373
|
|---|---|
| Preferred Name | ADA2 protein, human |
| Synonyms |
CECR1 protein, human
cat eye syndrome chromosome region, candidate 1 protein, human
adenosine deaminase 2, human
ADA2 adenosine deaminase, human
|
| Type | http://www.w3.org/2002/07/owl#Class |
All Properties
| altLabel |
CECR1 protein, human
cat eye syndrome chromosome region, candidate 1 protein, human
adenosine deaminase 2, human
ADA2 adenosine deaminase, human
|
|---|---|
| prefLabel | ADA2 protein, human
|
| Scope Statement | RefSeq NM_177405. Mutations in the ADA2 protein, human genes are associated with Sneddon Syndrome and deficiency of adenosine deaminase 2.
|
| type | |
| tui |
T116
T126
|
| HM |
D000243
D036341
|
| SC | 1
|
| TERMUI |
T509062
T776936
T856640
T509063
T286802
|
| TH |
NLM (1996)
NLM (2002)
NLM (2010)
NLM (2014)
|
| SRC | Genomics 2000 Mar 15;64(3):277-85
|
| MMR | 20221102
|
| notation | C408373
|
| Semantic type UMLS property | |
| cui | C0914385
|
| MeSH Frequency | 147
|
| PI | *GROWTH SUBSTANCES (2000-2002)
|
| DSC | 20000526
|
| Inverse of RB | EC 3.5.4.4
|
| Mapped to | |
| MDA | 20000526
|
| Delete | Subject | Author | Type | Created |
|---|---|---|---|---|
| No notes to display |