DOID:3490
|
-
Noonan syndrome
-
Aliases:
-
Turner's phenotype, karyotype normal
|
|
|
Mus musculus (house mouse)
|
|
DOID:0060903
|
|
|
|
Mus musculus (house mouse)
|
|
DOID:0112243
|
-
congenital symmetric circumferential skin creases 2
-
Aliases:
|
|
|
Homo sapiens (human)
|
|
DOID:0111953
|
-
immunodeficiency 23
-
Aliases:
-
CID due to PGM3 deficiency
-
IMD23
-
PGM3-CDG
-
PGM3-related congenital disorder of glycosylation
-
combined immunodeficiency due to PGM3 deficiency
|
|
|
Mus musculus (house mouse)
|
|
DOID:3307
|
|
|
|
Mus musculus (house mouse)
|
|
DOID:0060308
|
-
autosomal recessive intellectual developmental disorder
-
Aliases:
-
autosomal recessive mental retardation
-
autosomal recessive non-syndromic mental retardation
|
|
|
Homo sapiens (human)
|
|
DOID:0060180
|
|
|
|
Mus musculus (house mouse)
|
|
DOID:0050824
|
-
sinoatrial node disease
-
Aliases:
|
|
|
Mus musculus (house mouse)
|
|
DOID:0111700
|
-
ankyrin-B-related cardiac arrhythmia
-
Aliases:
|
|
|
Mus musculus (house mouse)
|
|
DOID:13884
|
-
sick sinus syndrome
-
Aliases:
|
|
|
Mus musculus (house mouse)
|
|
DOID:224
|
-
transient cerebral ischemia
-
Aliases:
-
TIA
-
TIA - Transient ischaemic attack
-
Transient cerebral ischaemia
-
Transient ischemic attacks
-
transient ischemic attack
|
|
|
Mus musculus (house mouse)
|
|
DOID:0060224
|
-
atrial fibrillation
-
Aliases:
|
|
|
Mus musculus (house mouse)
|
|
DOID:2843
|
-
long QT syndrome
-
Aliases:
|
|
|
Mus musculus (house mouse)
|
|
DOID:12849
|
-
autistic disorder
-
Aliases:
-
Kanner's syndrome
-
autism
-
autistic disorder of childhood onset
-
childhood autism
-
infantile autism
|
|
|
Mus musculus (house mouse)
|
|
DOID:3717
|
-
gastric adenocarcinoma
-
Aliases:
-
adenocarcinoma of stomach
-
stomach adenocarcinoma
|
|
|
Homo sapiens (human)
|
|
DOID:0080962
|
|
|
|
Homo sapiens (human)
|
|
DOID:0080686
|
-
tubular aggregate myopathy 2
|
|
|
Mus musculus (house mouse)
|
|
DOID:0111976
|
-
immunodeficiency 9
-
Aliases:
-
CID due to ORAI1 deficiency
-
IMD9
-
combined immunodeficiency due to ORAI1 deficiency
-
immune dysfunction with T-cell inactivation due to calcium entry defect 1
|
|
|
Mus musculus (house mouse)
|
|
DOID:12930
|
-
dilated cardiomyopathy
-
Aliases:
-
primary dilated cardiomyopathy
|
|
|
Mus musculus (house mouse)
|
|
DOID:11984
|
-
hypertrophic cardiomyopathy
-
Aliases:
-
hypertrophic obstructive cardiomyopathy
|
|
|
Mus musculus (house mouse)
|
|
DOID:0050873
|
|
|
|
Mus musculus (house mouse)
|
|
DOID:0060352
|
-
Kleefstra syndrome 1
-
Aliases:
-
9q subtelomeric deletion syndrome
-
9q-syndrome
-
9q34 deletion syndrome
|
|
|
Homo sapiens (human)
|
|
DOID:986
|
|
|
|
Homo sapiens (human)
|
|
DOID:0050156
|
-
idiopathic pulmonary fibrosis
-
Aliases:
-
FIBROCYSTIC PULMONARY DYSPLASIA
-
IDIOPATHIC PULMONARY FIBROSIS, FAMILIAL
-
cryptogenic fibrosing alveolitis
|
|
|
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
|
|
|
Mus musculus (house mouse)
|
|