DOID:2215
|
-
factor VII deficiency
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:2583
|
-
agammaglobulinemia
-
Aliases:
-
IGHM
-
hypogammaglobulinemia
-
mu heavy chain deficiency
|
|
|
Homo sapiens (human)
|
|
DOID:11476
|
|
|
|
Homo sapiens (human)
|
|
DOID:4971
|
-
myelofibrosis
-
Aliases:
-
Agnogenic myeloid metaplasia
-
Aleukemic myelosis
-
Megakaryocytic myelosclerosis
-
bone Marrow Fibrosis
-
myelosclerosis
-
primary myelofibrosis
|
|
|
Homo sapiens (human)
|
|
DOID:4090
|
-
agnosia
-
Aliases:
-
Dyspraxia
-
Dyspraxia syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:593
|
|
|
|
Homo sapiens (human)
|
|
DOID:0050590
|
-
severe congenital neutropenia
|
|
|
Homo sapiens (human)
|
|
DOID:1227
|
|
|
|
Homo sapiens (human)
|
|
DOID:12987
|
-
agranulocytosis
-
Aliases:
-
Granulocytopenic disorder
-
Granulopenia
-
granulocytopenia
|
|
|
Homo sapiens (human)
|
|
DOID:4267
|
|
|
|
Homo sapiens (human)
|
|
DOID:2749
|
-
glycogen storage disease Ia
|
|
|
Homo sapiens (human)
|
|
DOID:9870
|
-
galactosemia
-
Aliases:
-
Galactosaemia
-
Galactose intolerance
|
|
|
Homo sapiens (human)
|
|
DOID:9266
|
|
|
|
Homo sapiens (human)
|
|
DOID:2747
|
-
glycogen storage disease
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:2862
|
-
glucosephosphate dehydrogenase deficiency
-
Aliases:
-
Glucose-6-phosphate dehydrogenase deficiency
-
deficiency of G-6PD
|
|
|
Homo sapiens (human)
|
|
DOID:0050632
|
|
|
|
Homo sapiens (human)
|
|
DOID:0060831
|
-
Griscelli syndrome
-
Aliases:
-
Chediak-Higashi-like syndrome
-
Griscelli-Prunieras syndrome
-
partial albinism-immunodeficiency syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:0060833
|
-
Griscelli syndrome type 2
-
Aliases:
-
GS2
-
Griscelli syndrome with hemophagocytic syndrome
-
Griscelli-Prunieras syndrome type 2
-
PAID syndrome
-
hypopigmentation-immunodeficiency with or without neurologic impairment syndrome
-
partial albinism and immunodeficiency syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:0060834
|
-
Griscelli syndrome type 3
-
Aliases:
-
GS3
-
Griscelli-Prunieras syndrome type 3
|
|
|
Homo sapiens (human)
|
|
DOID:0110949
|
-
Waardenburg syndrome type 3
-
Aliases:
-
Klein-Waardenburg syndrome
-
WS3
-
Waardenburg syndrome type III
-
Waardenburg syndrome with upper limb anomalies
|
|
|
Homo sapiens (human)
|
|
DOID:0090100
|
-
ocular albinism with sensorineural deafness
-
Aliases:
-
WS2-OA
-
autosomal recessive Waardenburg syndrome type 2 with ocular albinism
-
digenic Waardenburg syndrome/albinism
-
digenic Waardenburg syndrome/ocular albinism
|
|
|
Homo sapiens (human)
|
|
DOID:0060832
|
-
Griscelli syndrome type 1
-
Aliases:
-
GS1
-
Griscelli syndrome with neurological impairment
-
Griscelli syndrome, cutaneous and neurological type
-
Griscelli-Prunieras syndrome type 1
-
hypopigmentation-neurologic impairment syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:576
|
|
|
|
Homo sapiens (human)
|
|
DOID:0050741
|
-
alcohol dependence
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:1574
|
-
alcohol use disorder
-
Aliases:
-
Ethanol abuse
-
alcohol abuse
|
|
|
Homo sapiens (human)
|
|