DOID:9252
|
-
amino acid metabolic disorder
-
Aliases:
-
inborn errors of amino acid metabolism
|
|
|
Homo sapiens (human)
|
|
DOID:10914
|
-
amnestic disorder
-
Aliases:
-
Amnestic syndrome
-
Korsakoff's psychosis or syndrome
-
amnesia
|
|
|
Homo sapiens (human)
|
|
DOID:11037
|
-
dissociative amnesia
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:4543
|
|
|
|
Homo sapiens (human)
|
|
DOID:9120
|
|
|
|
Homo sapiens (human)
|
|
DOID:318
|
-
progressive muscular atrophy
-
Aliases:
-
Pure progressive muscular atrophy
-
progressive spinal muscular atrophy
|
|
|
Homo sapiens (human)
|
|
DOID:332
|
-
amyotrophic lateral sclerosis
-
Aliases:
-
ALS
-
Lou Gehrig's disease
-
motor neuron disease, bulbar
|
|
|
Homo sapiens (human)
|
|
DOID:2355
|
|
|
|
Homo sapiens (human)
|
|
DOID:2361
|
-
macrocytic anemia
-
Aliases:
-
ANEMIA MACROCYTIC
-
Macrocytic anaemia
|
|
|
Homo sapiens (human)
|
|
DOID:12449
|
|
|
|
Homo sapiens (human)
|
|
DOID:12241
|
|
|
|
Homo sapiens (human)
|
|
DOID:1338
|
-
congenital dyserythropoietic anemia
-
Aliases:
-
congenital dyshaematopoietic anaemia
|
|
|
Homo sapiens (human)
|
|
DOID:583
|
-
hemolytic anemia
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:1098
|
-
fetal erythroblastosis
-
Aliases:
-
EF - Erythroblastosis foetalis
-
Haemolytic disease due to rhesus isoimmunisation
-
erythroblastosis fetalis
-
rhesus isoimmunisation of the newborn
|
|
|
Homo sapiens (human)
|
|
DOID:718
|
-
autoimmune hemolytic anemia
-
Aliases:
-
Autoimmune haemolytic anaemia
-
autoimmune hemolytic anaemia
|
|
|
Homo sapiens (human)
|
|
DOID:13628
|
|
|
|
Homo sapiens (human)
|
|
DOID:589
|
-
congenital hemolytic anemia
-
Aliases:
-
congenital hemolytic anaemia
-
hereditary hemolytic anaemia
-
hereditary hemolytic anemia
|
|
|
Homo sapiens (human)
|
|
DOID:2373
|
-
hereditary elliptocytosis
-
Aliases:
-
Congenital elliptocytosis
-
ovalocytosis
|
|
|
Homo sapiens (human)
|
|
DOID:2860
|
-
hemoglobinopathy
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:2861
|
-
congenital nonspherocytic hemolytic anemia
-
Aliases:
-
HNSHA
-
congenital nonspherocytic hemolytic anaemia
-
hereditary nonspherocytic hemolytic anaemia
-
hereditary nonspherocytic hemolytic anemia
|
|
|
Homo sapiens (human)
|
|
DOID:13382
|
-
megaloblastic anemia
-
Aliases:
-
Grasbeck-Imerslund syndrome
-
Imerslund-Grasbeck syndrome
-
MGA1 Norwegian type
-
RH-MGA1
-
megaloblastic anaemia
-
recessive hereditary megaloblastic anaemia 1
-
recessive hereditary megaloblastic anemia 1
|
|
|
Homo sapiens (human)
|
|
DOID:11244
|
-
neonatal anemia
-
Aliases:
-
anaemia neonatal
-
anemia neonatal
-
neonatal anaemia
|
|
|
Homo sapiens (human)
|
|
DOID:13381
|
-
pernicious anemia
-
Aliases:
-
ANEMIA PERNICIOUS
-
Addison's anaemia
-
Biermer's anaemia
-
Biermer's anemia
-
pernicious anaemia
|
|
|
Homo sapiens (human)
|
|
DOID:10923
|
-
sickle cell anemia
-
Aliases:
-
Hb SC disease
-
Hb-S/Hb-C disease
-
Hb-SS disease without crisis
-
Hemoglobin S disease without crisis
-
Sickle-cell/Hb-C disease without crisis
-
drepanocytosis
-
haemoglobin SC disease
-
hemoglobin SC disease
-
sickle cell anaemia
|
|
|
Homo sapiens (human)
|
|
DOID:8955
|
-
sideroblastic anemia
-
Aliases:
-
ANEMIA SIDEROBLASTIC
-
Anemia, hypochromic with iron loading
|
|
|
Homo sapiens (human)
|
|