DOID:2703
|
|
|
|
Homo sapiens (human)
|
DOID:970
|
-
tenosynovitis
-
Aliases:
-
Inflammation of tendon sheath
|
|
|
Homo sapiens (human)
|
DOID:3347
|
-
osteosarcoma
-
Aliases:
-
Osteogenic sarcoma
-
Skeletal sarcoma
-
bone tissue neoplasm
-
osteoid sarcoma
|
|
|
Homo sapiens (human)
|
DOID:3376
|
-
bone osteosarcoma
-
Aliases:
-
Osteosarcoma of bone
-
primary Osteosarcoma of bone
|
|
|
Homo sapiens (human)
|
DOID:204
|
|
|
|
Homo sapiens (human)
|
DOID:3361
|
-
childhood osteosarcoma
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0110721
|
-
neuronal ceroid lipofuscinosis 1
-
Aliases:
-
CLN1
-
neuronal ceroid lipofuscinosis 1 variable age of onset
|
|
|
Homo sapiens (human)
|
DOID:14503
|
-
neuronal ceroid lipofuscinosis
-
Aliases:
-
hereditary ceroid lipofuscinosis
|
|
|
Homo sapiens (human)
|
DOID:0110729
|
-
neuronal ceroid lipofuscinosis 6A
-
Aliases:
-
CLN6
-
neuronal ceroid lipofuscinosis 6
-
neuronal ceroid lipofuscinosis 6 variable age of onset
|
|
|
Homo sapiens (human)
|
DOID:0110724
|
-
neuronal ceroid lipofuscinosis 8 northern epilepsy variant
-
Aliases:
-
EPMR
-
northern epilepsy variant, neuronal ceroid lipofuscinosis, Northern epilepsy variant
-
progressive epilepsy with mental retardation, northern epilepsy
-
progressive epilepsy-intellectual disability syndrome, Finnish type
|
|
|
Homo sapiens (human)
|
DOID:0110726
|
-
neuronal ceroid lipofuscinosis 2
-
Aliases:
-
CLN2
-
neuronal ceroid lipofuscinosis 2 variable age at onset
|
|
|
Homo sapiens (human)
|
DOID:0110720
|
-
neuronal ceroid lipofuscinosis 4
-
Aliases:
-
CLN4B disease
-
autosomal dominant neuronal ceroid lipofuscinosis 4B
-
neuronal ceroid lipofuscinosis 4 Parry type
-
neuronal ceroid lipofuscinosis 4B
|
|
|
Homo sapiens (human)
|
DOID:0110732
|
-
neuronal ceroid lipofuscinosis 11
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0110731
|
-
neuronal ceroid lipofuscinosis 3
-
Aliases:
-
Batten disease
-
CLN3
-
juvenile neuronal ceroid lipofuscinosis
|
|
|
Homo sapiens (human)
|
DOID:0110727
|
-
neuronal ceroid lipofuscinosis 13
-
Aliases:
-
CLN13
-
neuronal ceroid lipofuscinosis 13 Kufs type
|
|
|
Homo sapiens (human)
|
DOID:0110728
|
-
neuronal ceroid lipofuscinosis 5
-
Aliases:
-
CLN5
-
neuronal ceroid lipofuscinosis 5 variable age of onset
|
|
|
Homo sapiens (human)
|
DOID:0110725
|
-
neuronal ceroid lipofuscinosis 10
-
Aliases:
-
CLN10
-
Cathepsin D deficiency
-
neuronal ceroid lipofuscinosis cathepsin D-deficient
-
neuronal ceroid lipofuscinosis due to cathepsin D deficiency
|
|
|
Homo sapiens (human)
|
DOID:0110723
|
-
neuronal ceroid lipofuscinosis 8
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0110733
|
-
neuronal ceroid lipofuscinosis 9
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0110722
|
-
neuronal ceroid lipofuscinosis 7
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0110730
|
-
neuronal ceroid lipofuscinosis 6B
-
Aliases:
-
CLN4A
-
autosomal recessive neuronal ceroid lipofuscinosis 4A
-
neuronal ceroid lipofuscinosis 4A
|
|
|
Homo sapiens (human)
|
DOID:350
|
|
|
|
Homo sapiens (human)
|
DOID:7912
|
-
mixed oligodendroglioma-astrocytoma
-
Aliases:
-
WHO grade II mixed glioma
|
|
|
Homo sapiens (human)
|
DOID:9254
|
|
|
|
Homo sapiens (human)
|
DOID:3181
|
-
oligodendroglioma
-
Aliases:
-
oligodendroglial neoplasm
-
oligodendroglial tumor
|
|
|
Homo sapiens (human)
|