DOID:3112
|
-
papillary adenocarcinoma
-
Aliases:
-
Infiltrating and papillary adenocarcinoma
-
infiltrating papillary adenocarcinoma
|
|
|
Homo sapiens (human)
|
DOID:3969
|
-
thyroid gland papillary carcinoma
-
Aliases:
-
Papillary carcinoma of the Thyroid gland
|
|
|
Homo sapiens (human)
|
DOID:7442
|
-
monoclonal gammopathy of uncertain significance
-
Aliases:
-
MGUS
-
Monoclonal gammopathy of undetermined significance
|
|
|
Homo sapiens (human)
|
DOID:0080001
|
|
|
|
Homo sapiens (human)
|
DOID:1222
|
-
cartilage disease
-
Aliases:
-
Cartilage disorder
-
Chondropathy
|
|
|
Homo sapiens (human)
|
DOID:65
|
-
connective tissue disease
-
Aliases:
-
connective tissue disorder
-
disorder of connective tissue
|
|
|
Homo sapiens (human)
|
DOID:0060284
|
-
paroxysmal nocturnal hemoglobinuria
|
|
|
Homo sapiens (human)
|
DOID:1340
|
-
pure red-cell aplasia
-
Aliases:
-
Red cell hypoplasia
-
primary red cell aplasia
-
pure red cell aplasia
|
|
|
Homo sapiens (human)
|
DOID:14723
|
-
beta-ketothiolase deficiency
-
Aliases:
-
2-methyl-3-hydroxybutyricacidemia
-
3-ketothiolase deficiency
-
3-oxothiolase deficiency
-
Mitochondrial acetoacetyl-CoA Thiolase deficiency
-
alpha-methylacetoaceticaciduria
-
peroxisomal thiolase deficiency
|
|
|
Homo sapiens (human)
|
DOID:718
|
-
autoimmune hemolytic anemia
-
Aliases:
-
Autoimmune haemolytic anaemia
-
autoimmune hemolytic anaemia
|
|
|
Homo sapiens (human)
|
DOID:1923
|
-
disorder of sexual development
-
Aliases:
-
sex development disorder
-
sex differentiation disease
|
|
|
Homo sapiens (human)
|
DOID:3763
|
|
|
|
Homo sapiens (human)
|
DOID:3765
|
-
pseudohermaphroditism
-
Aliases:
-
Indeterminate sex and pseudohermaphroditism
|
|
|
Homo sapiens (human)
|
DOID:0050127
|
|
|
|
Mus musculus (house mouse)
|
DOID:2841
|
-
asthma
-
Aliases:
-
bronchial hyperreactivity
-
chronic obstructive asthma
-
chronic obstructive asthma with acute exacerbation
-
chronic obstructive asthma with status asthmaticus
|
|
|
Mus musculus (house mouse)
|
DOID:8456
|
-
choline deficiency disease
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:9263
|
-
homocystinuria
-
Aliases:
-
CBS deficiency
-
cystathionine beta synthase deficiency
-
cystathionine synthase deficiency
|
|
|
Homo sapiens (human)
|
DOID:0050729
|
-
Chanarin-Dorfman syndrome
-
Aliases:
-
neutral lipid storage disease
|
|
|
Homo sapiens (human)
|
DOID:14250
|
-
Down syndrome
-
Aliases:
-
Complete trisomy 21 syndrome
-
Down's syndrome
-
Down's syndrome - trisomy 21
-
Downs syndrome
-
G Trisomy
-
trisomy 21 syndrome
|
|
|
Homo sapiens (human)
|
DOID:1272
|
|
|
|
Homo sapiens (human)
|
DOID:1271
|
-
capillary disease
-
Aliases:
|
|
|
Homo sapiens (human)
|
DOID:1270
|
-
hereditary hemorrhagic telangiectasia
-
Aliases:
-
Osler hemorrhagic telangiectasia syndrome
-
Osler-Weber-Rendu disease
-
Rendu-Osler-Weber disease
|
|
|
Homo sapiens (human)
|
DOID:8337
|
-
appendicitis
-
Aliases:
-
acute appendicitis
-
acute appendicitis with generalized peritonitis
-
acute appendicitis with peritoneal abscess
|
|
|
Homo sapiens (human)
|
DOID:8729
|
-
milker's nodule
-
Aliases:
-
Milkers' node
-
Paravaccinia
-
milker nodule
|
|
|
Homo sapiens (human)
|
DOID:0050508
|
|
|
|
Homo sapiens (human)
|