DOID:0070027
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CST3-related cerebral amyloid angiopathy
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Aliases:
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Amyloidosis VI
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Amyloidosis, Cerebroarterial, Icelandic Type
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Cerebral Hemorrhage, Hereditary, with Amyloidosis, Icelandic Variant
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HCHWA
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Hereditary Cerebral Hemorrhage with Amyloidosis, Icelandic Variant
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Homo sapiens (human)
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DOID:0070025
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X-linked dyskeratosis congenita
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Aliases:
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DKCX
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Zinsser-Cole-Engman syndrome
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Homo sapiens (human)
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DOID:0070014
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autosomal dominant dyskeratosis congenita 1
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Aliases:
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DKCA1
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Dyskeratosis Congenita, Scoggins Type
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Homo sapiens (human)
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DOID:0070004
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Homo sapiens (human)
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DOID:0060911
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karyomegalic interstitial nephritis
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Aliases:
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Homo sapiens (human)
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DOID:0060903
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Homo sapiens (human)
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DOID:0060901
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lymphoplasmacytic lymphoma
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Aliases:
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Waldenstroem's macroglobulinemia
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Waldenstrom Macroglobulinemia
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lymphoplasmacytic lymphoma with IgM gammopathy
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Homo sapiens (human)
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DOID:0060900
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Parkinson's disease 14
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Aliases:
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Dystonia-Parkinsonism Adult-Onset
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autosomal recessive Parkinson disease 14
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autosomal recessive Parkinson's disease 14
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|
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Homo sapiens (human)
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DOID:0060898
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Parkinson's disease 20
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Aliases:
-
early-onset Parkinson disease 20
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early-onset Parkinson's disease 20
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|
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Homo sapiens (human)
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DOID:0060896
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-
Parkinson's disease 23
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Aliases:
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autosomal recessive early-onset Parkinson disease 23
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autosomal recessive early-onset Parkinson's disease 23
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|
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Homo sapiens (human)
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DOID:0060895
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Parkinson's disease 4
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Aliases:
-
autosomal dominant Lewy body Parkinson disease 4
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autosomal dominant Parkinson disease 4
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autosomal dominant Parkinson's disease 4
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Homo sapiens (human)
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DOID:0060894
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early-onset Parkinson's disease
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Aliases:
-
early-onset Parkinson disease
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|
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Homo sapiens (human)
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DOID:0060892
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late onset Parkinson's disease
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Aliases:
-
late onset Parkinson disease
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Homo sapiens (human)
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DOID:0060892
|
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late onset Parkinson's disease
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Aliases:
-
late onset Parkinson disease
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Mus musculus (house mouse)
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DOID:0060892
|
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late onset Parkinson's disease
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Aliases:
-
late onset Parkinson disease
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|
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Caenorhabditis elegans
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|
DOID:0060891
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Parkinson's disease 19A
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Aliases:
-
juvenile onset Parkinson disease 19A
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juvenile onset Parkinson's disease 19A
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Homo sapiens (human)
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DOID:0060890
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ectopic Cushing syndrome
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Aliases:
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Cushing syndrome due to ectopic ACTH secretion
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ectopic ACTH secreting tumor
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|
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Homo sapiens (human)
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DOID:0060889
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prune belly syndrome
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Aliases:
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Eagle-Barret syndrome
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Obrisnksy syndrome
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abdominal muscle deficiency syndrome
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|
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Homo sapiens (human)
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|
DOID:0060888
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transient myeloproliferative syndrome
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Aliases:
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MST
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TAM
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transient abnormal myelopoiesis
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transient leukemia
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transient leukemia of Down syndrome
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transient myeloproliferative disease
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|
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Homo sapiens (human)
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|
DOID:0060887
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ossification of the posterior longitudinal ligament of spine
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Aliases:
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|
|
Mus musculus (house mouse)
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|
DOID:0060887
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ossification of the posterior longitudinal ligament of spine
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Aliases:
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|
|
Homo sapiens (human)
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|
DOID:0060887
|
-
ossification of the posterior longitudinal ligament of spine
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Aliases:
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|
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Rattus norvegicus (Norway rat)
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|
DOID:0060878
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hypoparathyroidism-deafness-renal disease syndrome
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Aliases:
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Barakat syndrome
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HDR syndrome
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hypoparathyroidism, sensorineural deafness, and renal disease
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|
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Homo sapiens (human)
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|
DOID:0060877
|
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bullous congenital ichthyosiform erythroderma
-
Aliases:
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bullous type ichthyosis
-
ichthyosis bullosa of Siemens
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superficial epidermolytic ichthyosis
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|
|
Homo sapiens (human)
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|
DOID:0060875
|
-
isolated growth hormone deficiency type III
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Aliases:
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Fleisher syndrome
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IGHD III
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X-linked IGHD
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X-linked agammaglobulinemia and isolated growth hormone deficiency
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X-linked hypogammaglobulinemia and isolated growth hormone deficiency
-
X-linked isolated growth hormone deficiency
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congenital IGHD type III
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congenital isolated GH deficiency type III
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congenital isolated growth hormone deficiency type III
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growth hormone deficiency with hypogammaglobulinemia
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|
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Homo sapiens (human)
|
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