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loading...| Preferred Name |
Acrodermatitis enteropathica |
| Synonyms |
Acrodermatitis enteropathica zinc deficiency type |
| ID |
http://purl.bioontology.org/ontology/MESH/C538178 |
| altLabel |
Acrodermatitis enteropathica zinc deficiency type Acrodermatitis Enteropathica, Zinc-Deficiency Type |
| cui |
C0221036 |
| Has mapping qualifier | |
| HM |
D015032/Q000172 D000169 |
| Inverse of RB |
0 |
| Mapped to | |
| MDA |
20100625 |
| MeSH Frequency |
189 |
| MMR |
20150817 |
| notation |
C538178 |
| prefLabel |
Acrodermatitis enteropathica |
| SC |
3 |
| Scope Statement |
A disorder of ZINC metabolism that can either be inherited or acquired. In both cases, zinc is not absorbed from the intestine, resulting in pustular DERMATITIS; DIARRHEA, and nail dystrophy. Emotional disturbances may also occur. The inherited form is caused by mutations in the SLC39A4 gene. The acquired form can result from diets lacking the appropriate amount of zinc. OMIM: 201100 |
| TERMUI |
T744979 T744978 T800737 |
| TH |
ORD (2010) OMIM (2013) |
| tui |
T047 |
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