C0009714 |
Hepatic Fibrosis, Congenital |
DO |
polycystic kidney disease 4
|
0080212 |
C0009714 |
Hepatic Fibrosis, Congenital |
DO |
autosomal recessive polycystic kidney disease
|
0110861 |
C0009714 |
Hepatic Fibrosis, Congenital |
HPO |
Congenital hepatic fibrosis
|
HP:0002612 |
C0009714 |
Hepatic Fibrosis, Congenital |
HPO |
Excessive buildup of connective tissue and scarring of liver at birth
|
HP:0002612 |
C0009714 |
Hepatic Fibrosis, Congenital |
MONDO |
congenital hepatic fibrosis
|
0022263 |
C0009714 |
Hepatic Fibrosis, Congenital |
MONDO |
polycystic kidney disease 4
|
0033004 |
C0009714 |
Hepatic Fibrosis, Congenital |
MSH |
Hepatic Fibrosis, Congenital
|
C562378 |
C0009714 |
Hepatic Fibrosis, Congenital |
NCI |
Congenital Hepatic Fibrosis
|
C97071 |
C0009714 |
Hepatic Fibrosis, Congenital |
OMIM |
HEPATIC FIBROSIS, CONGENITAL
|
263200 |
C0009714 |
Hepatic Fibrosis, Congenital |
OMIM |
POLYCYSTIC KIDNEY DISEASE 4 WITH OR WITHOUT POLYCYSTIC LIVER DISEASE
|
263200 |
C0009714 |
Hepatic Fibrosis, Congenital |
OMIM |
POLYCYSTIC KIDNEY DISEASE, AUTOSOMAL RECESSIVE
|
263200 |