Jump to:
loading...| Preferred Name | CIRRHOSIS, FAMILIAL | |
| Synonyms |
CIRRHOSIS, NONCRYPTOGENIC, SUSCEPTIBILITY TO COPPER TOXICOSIS, IDIOPATHIC CIRRHOSIS, FAMILIAL, WITH PULMONARY HYPERTENSION INDIAN CHILDHOOD CIRRHOSIS ICT COPPER-OVERLOAD CIRRHOSIS ENDEMIC TYROLEAN INFANTILE CIRRHOSIS ICC CIRRHOSIS, CRYPTOGENIC ETIC SEN SYNDROME |
|
| ID |
http://purl.bioontology.org/ontology/OMIM/215600 |
|
| altLabel |
CIRRHOSIS, NONCRYPTOGENIC, SUSCEPTIBILITY TO COPPER TOXICOSIS, IDIOPATHIC CIRRHOSIS, FAMILIAL, WITH PULMONARY HYPERTENSION INDIAN CHILDHOOD CIRRHOSIS ICT COPPER-OVERLOAD CIRRHOSIS ENDEMIC TYROLEAN INFANTILE CIRRHOSIS ICC CIRRHOSIS, CRYPTOGENIC ETIC SEN SYNDROME |
|
| cui |
C1876166 C0267809 C0268074 C1861556 C1859088 C1835713 C1876165 |
|
| Gene Locus |
12q13 |
|
| Gene Symbol |
KRT18 |
|
| MIMTYPEMEANING |
Phenotype description, molecular basis known. |
|
| notation |
215600 |
|
| OMIM Entry Type |
3 |
|
| OMIM MimType Value |
pound |
|
| prefLabel |
CIRRHOSIS, FAMILIAL |
|
| tui |
T047 T033 |
Create mapping