DOID:3328
|
-
temporal lobe epilepsy
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:11476
|
|
|
|
Homo sapiens (human)
|
|
DOID:6262
|
-
follicular dendritic cell sarcoma
-
Aliases:
-
Follicular Dendritic cell sarcoma
-
Follicular dendritic cell tumour
|
|
|
Homo sapiens (human)
|
|
DOID:5132
|
-
leiomyoma cutis
-
Aliases:
-
Cutaneous leiomyoma
-
leiomyoma of the skin
|
|
|
Homo sapiens (human)
|
|
DOID:2773
|
-
contact dermatitis
-
Aliases:
-
Contact dermatitis/eczema
-
Contact eczema
-
Dermatitis, venenata
-
dermatitis venenata
|
|
|
Homo sapiens (human)
|
|
DOID:0110475
|
-
autosomal recessive nonsyndromic deafness 1A
-
Aliases:
-
DFNB1A
-
autosomal recessive deafness 1A
|
|
|
Homo sapiens (human)
|
|
DOID:350
|
|
|
|
Homo sapiens (human)
|
|
DOID:10914
|
-
amnestic disorder
-
Aliases:
-
Amnestic syndrome
-
Korsakoff's psychosis or syndrome
-
amnesia
|
|
|
Homo sapiens (human)
|
|
DOID:0112318
|
-
Schindler disease type 1
-
Aliases:
-
NAGA deficiency type 1
-
alpha-N-acetylgalactosaminidase deficiency type 1
|
|
|
Homo sapiens (human)
|
|
DOID:720
|
-
normocytic anemia
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:5200
|
-
urinary tract obstruction
-
Aliases:
-
Obstructive Uropathy
-
urinary obstruction
|
|
|
Homo sapiens (human)
|
|
DOID:891
|
-
progressive myoclonus epilepsy
-
Aliases:
-
PME
-
progressive myoclonic epilepsy
|
|
|
Homo sapiens (human)
|
|
DOID:850
|
|
|
|
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:114
|
|
|
|
Homo sapiens (human)
|
|
DOID:11394
|
-
adult respiratory distress syndrome
-
Aliases:
-
ARDS
-
Non-cardiogenic pulmonary edema
-
Shock lung
-
acute respiratory distress syndrome
-
adult RDS
|
|
|
Homo sapiens (human)
|
|
DOID:0060695
|
-
hyperekplexia
-
Aliases:
-
Kok disease
-
congenital stiff man syndrome
-
familial startle disease
-
hereditary hyperekplexia
-
startle disease
|
|
|
Homo sapiens (human)
|
|
DOID:8771
|
-
contagious pustular dermatitis
-
Aliases:
-
Ecthyma contagiosum
-
Ecthyma, Contagious
-
Orf
-
scabby mouth
-
sheep pox
-
thistle disease
|
|
|
Homo sapiens (human)
|
|
DOID:0111235
|
-
congenital muscular dystrophy-dystroglycanopathy type A12
-
Aliases:
-
MDDGA12
-
Walker-Warburg syndrome or muscle-eye-brain disease POMK-related
-
congenital muscular dystrophy-dystroglycanopathy with brain and eye anomalies type A12
|
|
|
Homo sapiens (human)
|
|
DOID:7442
|
-
monoclonal gammopathy of uncertain significance
-
Aliases:
-
MGUS
-
Monoclonal gammopathy of undetermined significance
|
|
|
Homo sapiens (human)
|
|
DOID:1996
|
-
rectum adenocarcinoma
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:0110303
|
-
autosomal dominant limb-girdle muscular dystrophy type 1H
-
Aliases:
-
LGMD1H
-
muscular dystrophy limb-girdle type 1H
|
|
|
Homo sapiens (human)
|
|
DOID:9931
|
-
Waterhouse-Friderichsen syndrome
-
Aliases:
-
Meningococcal hemorrhagic adrenalitis
|
|
|
Homo sapiens (human)
|
|
DOID:0060298
|
-
complement component 4b deficiency
|
|
|
Homo sapiens (human)
|
|
DOID:2786
|
|
|
|
Homo sapiens (human)
|
|