DOID:3068
|
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glioblastoma
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Aliases:
-
GBM
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adult glioblastoma multiforme
-
glioblastoma multiforme
-
grade IV adult Astrocytic tumor
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primary glioblastoma multiforme
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spongioblastoma multiforme
|
|
|
Homo sapiens (human)
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|
DOID:0050527
|
-
obsolete familial hypertriglyceridemia
|
|
|
Homo sapiens (human)
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|
DOID:2224
|
-
essential thrombocythemia
-
Aliases:
-
Essential thrombocythaemia
-
familial thrombocytosis
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hemorrhagic thrombocythemia
-
hereditary thrombocythemia
-
primary Thrombocytosis
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|
|
Homo sapiens (human)
|
|
DOID:0060765
|
-
autosomal dominant Robinow syndrome 2
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Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:10071
|
-
larynx squamous papilloma
-
Aliases:
-
Laryngeal Squamous Cell Papilloma
|
|
|
Homo sapiens (human)
|
|
DOID:813
|
-
septic arthritis
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:0110572
|
-
autosomal dominant nonsyndromic deafness 49
-
Aliases:
-
DFNA49
-
autosomal dominant deafness 49
|
|
|
Homo sapiens (human)
|
|
DOID:0090103
|
-
Huntington's disease-like 1
-
Aliases:
-
HDL1
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HLN1
-
Huntington disease-like 1
-
Huntington-like neurodegenerative disorder 1
-
autosomal dominant Huntington-like neurodegenerative disorder
-
early-onset prion disease with prominent psychiatric features
|
|
|
Homo sapiens (human)
|
|
DOID:4305
|
-
bone giant cell tumor
-
Aliases:
-
Giant cell neoplasm of bone
-
Giant cell tumor of bone
-
Giant cell tumour of bone
-
bone giant cell tumour
|
|
|
Homo sapiens (human)
|
|
DOID:0060413
|
-
chromosome 22q11.2 deletion syndrome, distal
-
Aliases:
-
DiGeorge syndrome and Velocardiofacial syndrome
-
distal 22q11.2 microdeletion syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:331
|
-
central nervous system disease
|
|
|
Homo sapiens (human)
|
|
DOID:0110791
|
-
hereditary spastic paraplegia 3A
-
Aliases:
-
FSP1
-
SPG3A
-
autosomal dominant familial spastic paraplegia 1
-
autosomal dominant spastic paraplegia 3
-
autosomal dominant spastic paraplegia type 3
-
strumpell disease
|
|
|
Homo sapiens (human)
|
|
DOID:0070318
|
|
|
|
Homo sapiens (human)
|
|
DOID:0110915
|
-
childhood hypophosphatasia
|
|
|
Homo sapiens (human)
|
|
DOID:10608
|
-
celiac disease
-
Aliases:
-
celiac sprue
-
coeliac disease
-
idiopathic steatorrhea
|
|
|
Homo sapiens (human)
|
|
DOID:0110492
|
-
autosomal recessive nonsyndromic deafness 33
-
Aliases:
-
DFNB33
-
autosomal recessive deafness 33
|
|
|
Homo sapiens (human)
|
|
DOID:13910
|
-
red color blindness
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:3674
|
-
kidney rhabdoid cancer
-
Aliases:
-
renal Rhabdoid tumor
-
rhabdoid tumor of the kidney
|
|
|
Homo sapiens (human)
|
|
DOID:0050477
|
-
Liddle syndrome
-
Aliases:
-
Liddle's syndrome
-
Pseudoaldosteronism
|
|
|
Homo sapiens (human)
|
|
DOID:14693
|
-
Clouston syndrome
-
Aliases:
-
Clouston's hidrotic ectodermal dysplasia
-
Clouston's syndrome
-
Hidrotic ectodermal dysplasia syndrome
-
ectodermal dysplasia 2, Clouston type
-
hidrotic ectodermal dysplasia
|
|
|
Homo sapiens (human)
|
|
DOID:0060775
|
-
microvillus inclusion disease
-
Aliases:
-
Davidson disease
-
MVD
-
congenital familial protracted diarrhea with enterocyte brush-border abnormalities
-
congenital microvillus atrophy
-
diarrhea 2 with microvillus atrophy
-
intractable diarrhea of infancy
|
|
|
Homo sapiens (human)
|
|
DOID:0080171
|
-
esophageal atresia/tracheoesophageal fistula
-
Aliases:
-
esophageal atresia and/or tracheoesophageal fistula
-
tracheoesophageal fistula with or without esohageal atresia
|
|
|
Homo sapiens (human)
|
|
DOID:13068
|
-
renal osteodystrophy
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:12358
|
|
|
|
Homo sapiens (human)
|
|
DOID:9801
|
|
|
|
Homo sapiens (human)
|
|