DOID:14679
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Mus musculus (house mouse)
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DOID:0110765
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hereditary spastic paraplegia 12
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Aliases:
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SPG12
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autosomal dominant spastic paraplegia 12
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autosomal dominant spastic paraplegia type 12
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Mus musculus (house mouse)
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DOID:0070216
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familial hyperinsulinemic hypoglycemia 3
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Aliases:
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HHF3
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hyperinsulinemic hypoglycemia due to glucokinase deficiency
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hyperinsulinism due to glucokinase deficiency
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Mus musculus (house mouse)
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DOID:0111100
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maturity-onset diabetes of the young type 2
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Aliases:
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MODY glucokinase-related
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MODY type 2
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MODY2
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Mus musculus (house mouse)
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DOID:13317
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hyperinsulinemic hypoglycemia
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Aliases:
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Islet cell hyperplasia
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nesidioblastosis
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persistent hyperinsulinemia hypoglycemia of infancy
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Mus musculus (house mouse)
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DOID:11717
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neonatal diabetes
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Aliases:
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diabetes mellitus syndrome in newborn infant
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neonatal diabetes mellitus
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Mus musculus (house mouse)
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DOID:0050524
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maturity-onset diabetes of the young
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Aliases:
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Mus musculus (house mouse)
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DOID:0060639
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permanent neonatal diabetes mellitus
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Aliases:
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PDMI
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PNDM
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permanent diabetes mellitus of infancy
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Mus musculus (house mouse)
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DOID:4194
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glucose metabolism disease
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Aliases:
-
disorder of glucose metabolism
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Mus musculus (house mouse)
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DOID:9993
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Mus musculus (house mouse)
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DOID:4195
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Mus musculus (house mouse)
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DOID:11714
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gestational diabetes
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Aliases:
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GDM
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Gestational diabetes mellitus
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Maternal gestational diabetes mellitus
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Mus musculus (house mouse)
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DOID:2018
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Mus musculus (house mouse)
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DOID:9351
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diabetes mellitus
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Aliases:
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Mus musculus (house mouse)
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DOID:3393
|
-
coronary artery disease
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Aliases:
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CHD
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Coronary disease
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coronary arteriosclerosis
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coronary heart disease
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Mus musculus (house mouse)
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DOID:9352
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type 2 diabetes mellitus
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Aliases:
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NIDDM
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insulin resistance
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non-insulin-dependent diabetes mellitus
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type 2 diabetes
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type II diabetes mellitus
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Mus musculus (house mouse)
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DOID:10763
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hypertension
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Aliases:
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HTN
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hyperpiesia
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vascular hypertensive disorder
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Mus musculus (house mouse)
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DOID:0060610
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megacystis-microcolon-intestinal hypoperistalsis syndrome
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Aliases:
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Berdon syndrome
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Megacystis microcolon intestinal hypoperistalsis syndrome
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megacystis-microcolon-intestinal hypoperistalsis syndrome, MMIH
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visceral myopathy
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Homo sapiens (human)
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DOID:0080326
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familial hypertrophic cardiomyopathy
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Homo sapiens (human)
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DOID:0110186
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Charcot-Marie-Tooth disease type 4D
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Aliases:
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CMT4D
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Charcot-Marie-Tooth neuropathy type 4D
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HMSN Lom type
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HMSN-Lom
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HMSN4D
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HMSNL
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autosomal recessive demyelinating Charcot-Marie-Tooth disease type 4D
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hereditary motor and sensory neuropathy LOM type
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Homo sapiens (human)
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DOID:0070205
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familial partial lipodystrophy type 4
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Aliases:
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FPLD4
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PLIN1-related FPLD
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PLIN1-related familial partial lipodystrophy
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familial partial lipodystrophy associated with PLIN1 mutations
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Mus musculus (house mouse)
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DOID:0110197
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Charcot-Marie-Tooth disease dominant intermediate B
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Aliases:
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CMTDI1
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CMTDIB
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Charcot-Marie-Tooth neuropathy dominant intermediate B
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DI-CMTB
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Mus musculus (house mouse)
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|
DOID:0111223
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centronuclear myopathy 1
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Aliases:
|
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Mus musculus (house mouse)
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DOID:11252
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Mus musculus (house mouse)
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DOID:854
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collagen disease
-
Aliases:
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Mus musculus (house mouse)
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