DOID:11199
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Homo sapiens (human)
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DOID:0060856
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right atrial isomerism
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Aliases:
-
Ivemark syndrome
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asplenia with cardiovascular anomalies
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|
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Homo sapiens (human)
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DOID:0050731
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vitamin B12 deficiency
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Aliases:
-
cobalamin deficiency
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hypocobalaminemia
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Homo sapiens (human)
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DOID:10952
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Homo sapiens (human)
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DOID:0060001
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Homo sapiens (human)
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DOID:10935
|
-
dissociative disorder
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Aliases:
-
dissociative disease
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dissociative reaction
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|
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Homo sapiens (human)
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DOID:0050454
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-
periventricular nodular heterotopia
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Aliases:
-
periventricular heterotopia
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|
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Homo sapiens (human)
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DOID:850
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|
|
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Homo sapiens (human)
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DOID:255
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|
|
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Homo sapiens (human)
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DOID:0110178
|
-
Charcot-Marie-Tooth disease axonal type 2V
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Aliases:
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CMT2V
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Charcot-Marie-Tooth neuropathy type 2V
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autosomal dominant Charcot-Marie-Tooth disease type 2V
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autosomal dominant axonal Charcot-Marie-Tooth disease type 2V
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|
|
Homo sapiens (human)
|
DOID:6901
|
-
familiar ovarian carcinoma
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|
|
Homo sapiens (human)
|
DOID:0060676
|
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catecholaminergic polymorphic ventricular tachycardia 2
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Aliases:
|
|
|
Homo sapiens (human)
|
DOID:0050814
|
-
temtamy preaxial brachydactyly syndrome
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Aliases:
-
PREAXIAL BRACHYDACTYLY SYNDROME, TEMTAMY TYPE
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|
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Homo sapiens (human)
|
DOID:0080071
|
-
mucolipidosis III alpha/beta
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Aliases:
-
mucolipidosis III
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pseudo-Hurler polydystrophy
|
|
|
Homo sapiens (human)
|
DOID:3372
|
-
chondroblastic osteosarcoma
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Aliases:
-
chondrosarcomatous Osteogenic sarcoma
|
|
|
Homo sapiens (human)
|
DOID:1825
|
-
childhood absence epilepsy
-
Aliases:
-
petit mal seizure
-
pyknolepsy
|
|
|
Homo sapiens (human)
|
DOID:13258
|
|
|
|
Homo sapiens (human)
|
DOID:784
|
-
chronic kidney disease
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Aliases:
-
CKD
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CRF
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chronic kidney failure
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chronic renal disease
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chronic renal failure syndrome
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renal failure - chronic
|
|
|
Homo sapiens (human)
|
DOID:2634
|
|
|
|
Homo sapiens (human)
|
DOID:11555
|
-
Fuchs' endothelial dystrophy
-
Aliases:
-
FCED
-
Fuchs' corneal dystrophy
-
Fuchs' endothelial corneal dystrophy
|
|
|
Homo sapiens (human)
|
DOID:1080
|
-
filariasis
-
Aliases:
-
disease due to superfamily Filarioidea
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|
|
Homo sapiens (human)
|
DOID:2739
|
-
Gilbert syndrome
-
Aliases:
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Constitutional hyperbilirubinemia
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Gilbert's disease
-
Gilbert's syndrome
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Gilbert-Meulengracht syndrome
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hereditary nonhemolytic jaundice
|
|
|
Homo sapiens (human)
|
DOID:2571
|
-
Langerhans-cell histiocytosis
-
Aliases:
-
Histiocytosis X
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Langerhan's cell histiocytosis
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Langerhans cell granulomatosis
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Letterer-Siwe disease
-
Letterer-Siwe disease involving intra-abdominal lymph nodes
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Letterer-Siwe disease involving intrapelvic lymph nodes
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Letterer-Siwe disease involving intrathoracic lymph nodes
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Letterer-Siwe disease involving lymph nodes of axilla and upper limb
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Letterer-Siwe disease involving lymph nodes of head, face and neck
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Letterer-Siwe disease involving lymph nodes of head, face, and neck
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Letterer-Siwe disease involving lymph nodes of inguinal region and lower limb
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Letterer-Siwe disease involving lymph nodes of multiple sites
-
Letterer-Siwe disease involving spleen
-
Letterer-Siwe disease of intra-abdominal lymph nodes
-
Letterer-Siwe disease of intrapelvic lymph nodes
-
Letterer-Siwe disease of intrathoracic lymph nodes
-
Letterer-Siwe disease of lymph nodes of axilla and upper limb
-
Letterer-Siwe disease of lymph nodes of axilla and/or upper limb
-
Letterer-Siwe disease of lymph nodes of head, face and neck
-
Letterer-Siwe disease of lymph nodes of head, face and/or neck
-
Letterer-Siwe disease of lymph nodes of inguinal region amd/or lower limb
-
Letterer-Siwe disease of lymph nodes of inguinal region and lower limb
-
Letterer-Siwe disease of lymph nodes of inguinal region and/or lower limb
-
Letterer-Siwe disease of lymph nodes of multiple sites
-
Letterer-Siwe disease of spleen
|
|
|
Homo sapiens (human)
|
DOID:7188
|
-
autoimmune thyroiditis
-
Aliases:
-
Chronic Lymphocytic Thyroiditis
-
Hashimoto thyroiditis
-
Hashimoto's Disease
-
Hashimoto's syndrome
-
Hashimoto's thyroiditis
-
Lymphocytic Thyroiditis
|
|
|
Homo sapiens (human)
|
DOID:0060611
|
-
abdominal obesity-metabolic syndrome
|
|
|
Homo sapiens (human)
|