DOID:0081210
|
-
autosomal recessive intellectual developmental disorder 46
|
|
|
Homo sapiens (human)
|
|
DOID:0111045
|
-
platelet-type bleeding disorder 9
-
Aliases:
-
BDPLT9
-
GP Ia deficiency
-
collagen platelet receptor deficiency
-
glycoprotein Ia deficiency
|
|
|
Homo sapiens (human)
|
|
DOID:0110249
|
-
cataract 11 multiple types
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:9383
|
|
|
|
Homo sapiens (human)
|
|
DOID:0050536
|
-
obsolete SC phocomelia syndrome
-
Aliases:
-
Hypomelia Hypotrichosis Facial hemangioma syndrome
-
SC PSEUDOTHALIDOMIDE SYNDROME
|
|
|
Homo sapiens (human)
|
|
DOID:1227
|
|
|
|
Homo sapiens (human)
|
|
DOID:0070516
|
|
|
|
Homo sapiens (human)
|
|
DOID:0050904
|
|
|
|
Homo sapiens (human)
|
|
DOID:0081267
|
-
graft-versus-host disease
-
Aliases:
-
GvHD
-
graft versus host disease
|
|
|
Homo sapiens (human)
|
|
DOID:2986
|
-
IgA glomerulonephritis
-
Aliases:
-
Berger's IgA or IgG nephropathy
-
Focal Glomerulonephritis
-
IgA nephropathy
-
primary IgA nephropathy
-
segmental glomerulonephritis
|
|
|
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:1996
|
-
rectum adenocarcinoma
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:7442
|
-
monoclonal gammopathy of uncertain significance
-
Aliases:
-
MGUS
-
Monoclonal gammopathy of undetermined significance
|
|
|
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:114
|
|
|
|
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:10914
|
-
amnestic disorder
-
Aliases:
-
Amnestic syndrome
-
Korsakoff's psychosis or syndrome
-
amnesia
|
|
|
Homo sapiens (human)
|
|
DOID:0110475
|
-
autosomal recessive nonsyndromic deafness 1A
-
Aliases:
-
DFNB1A
-
autosomal recessive deafness 1A
|
|
|
Homo sapiens (human)
|
|
DOID:2773
|
-
contact dermatitis
-
Aliases:
-
Contact dermatitis/eczema
-
Contact eczema
-
Dermatitis, venenata
-
dermatitis venenata
|
|
|
Homo sapiens (human)
|
|
DOID:6262
|
-
follicular dendritic cell sarcoma
-
Aliases:
-
Follicular Dendritic cell sarcoma
-
Follicular dendritic cell tumour
|
|
|
Homo sapiens (human)
|
|
DOID:11476
|
|
|
|
Homo sapiens (human)
|
|
DOID:3328
|
-
temporal lobe epilepsy
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:4692
|
|
|
|
Homo sapiens (human)
|
|
DOID:4997
|
-
Camurati-Engelmann disease
-
Aliases:
-
Diaphyseal dysplasia
-
Engelman's disease
-
progressive diaphyseal dysplasia
|
|
|
Homo sapiens (human)
|
|
DOID:0111375
|
-
fetal akinesia deformation sequence syndrome
-
Aliases:
-
FADS
-
Pena-Shokeir syndrome type 1
-
arthrogryposis multiplex congenita-pulmonary hypoplasia syndrome
-
fetal akinesia sequence
-
foetal akinesia deformation sequence syndrome
-
foetal akinesia sequence
|
|
|
Homo sapiens (human)
|
|