DOID:5381
|
-
bile duct adenoma
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:1580
|
-
diffuse scleroderma
-
Aliases:
-
diffuse systemic sclerosis
-
systemic sclerosis, diffuse
|
|
|
Homo sapiens (human)
|
DOID:4660
|
-
indolent systemic mastocytosis
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0060075
|
-
estrogen-receptor positive breast cancer
|
|
|
Homo sapiens (human)
|
DOID:930
|
|
|
|
Homo sapiens (human)
|
DOID:11870
|
-
Pick's disease
-
Aliases:
-
Dementia in Pick's disease
-
LOBAR ATROPHY OF BRAIN
-
PICK DISEASE OF BRAIN
-
Pick disease
|
|
|
Homo sapiens (human)
|
DOID:0111057
|
-
platelet-type bleeding disorder 11
-
Aliases:
-
BDPLT11
-
GP VI deficiency
-
glycoprotein VI deficiency
|
|
|
Homo sapiens (human)
|
DOID:0111068
|
-
congenital bile acid synthesis defect 4
-
Aliases:
-
CBAS4
-
intrahepatic cholestasis with defective conversion of trihydroxycoprostanic acid to cholic acid
-
trihydroxycoprostanic acid in bile
|
|
|
Homo sapiens (human)
|
DOID:0110184
|
-
Charcot-Marie-Tooth disease type 4J
-
Aliases:
-
CMT4J
-
autosomal recessive Charcot-Marie-Tooth disease type 4J
|
|
|
Homo sapiens (human)
|
DOID:0050152
|
|
|
|
Homo sapiens (human)
|
DOID:9297
|
|
|
|
Homo sapiens (human)
|
DOID:9254
|
|
|
|
Homo sapiens (human)
|
DOID:2476
|
-
hereditary spastic paraplegia
-
Aliases:
-
French settlement disease
-
Strumpell-Lorrain disease
-
familial spastic paraplegia
-
hereditary spastic paraparesis
|
|
|
Homo sapiens (human)
|
DOID:0110271
|
-
cataract 23
-
Aliases:
-
CTRCT23
-
lamellar cataract 23
|
|
|
Homo sapiens (human)
|
DOID:0060784
|
-
ectrodactyly, ectodermal dysplasia, and cleft lip-palate syndrome 1
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:5363
|
-
myxoid liposarcoma
-
Aliases:
-
Myxoid/round cell liposarcoma
|
|
|
Homo sapiens (human)
|
DOID:0110175
|
-
Charcot-Marie-Tooth disease axonal type 2O
-
Aliases:
-
Charcot-Marie-Tooth neuropathy axonal type 2O
-
autosomal dominant Charcot-Marie-Tooth disease type 2O
-
autosomal dominant axonal Charcot-Marie-Tooth disease type 2O
|
|
|
Homo sapiens (human)
|
DOID:14501
|
-
Sjogren-Larsson syndrome
-
Aliases:
-
FALDH deficiency
-
SLS
-
Sjogren Larsson syndrome
-
Sjogren-Larsson's syndrome
-
fatty acid alcohol oxidoreductase deficiency
|
|
|
Homo sapiens (human)
|
DOID:0090129
|
-
carnitine palmitoyltransferase I deficiency
-
Aliases:
-
CPT I deficiency
-
CPT1A deficiency
-
L-CPT1 deficiency
-
carnitine palmitoyl transferase 1A deficiency
-
carnitine palmitoyl transferase IA deficiency
-
hepatic CPT deficiency type I
-
hepatic carnitine palmitoyl transferase 1 deficiency
-
hepatic carnitine palmitoyl transferase I deficiency
|
|
|
Homo sapiens (human)
|
DOID:0060708
|
-
lymphoproliferative syndrome 2
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:2748
|
-
glycogen storage disease III
-
Aliases:
-
Glycogen storage disease 3
-
Glycogen storage disease, type III
-
amylo 1,6 glucosidase deficiency
-
deficiency of debranching enzyme
-
deficiency of dextrin
|
|
|
Homo sapiens (human)
|
DOID:268
|
-
liver angiosarcoma
-
Aliases:
-
angiosarcoma of liver
-
hemangiosarcoma of the Liver
|
|
|
Homo sapiens (human)
|
DOID:8654
|
-
Hodgkin's lymphoma, mixed cellularity
-
Aliases:
-
Hodgkin's disease, mixed cellularity
|
|
|
Homo sapiens (human)
|
DOID:4305
|
-
bone giant cell tumor
-
Aliases:
-
Giant cell neoplasm of bone
-
Giant cell tumor of bone
-
Giant cell tumour of bone
-
bone giant cell tumour
|
|
|
Homo sapiens (human)
|
DOID:0080572
|
-
congenital disorder of glycosylation Iw
-
Aliases:
-
congenital disorder of glycosylation 1w
|
|
|
Homo sapiens (human)
|