|
Dandy-Walker syndrome
|
DOID_2785 |
[A cerebellar disease that is characterized by hypoplasia and upward rotation of the cerebellar vermis and cystic dilation of the fourth ventricle.] |
|
obsolete Ciliophora infectious disease
|
DOID_2788 |
[An Alveolata infectious disease that involves infection caused by the members of the phylum Ciliophora, which are characterized by the presence of hair-like organelles called cilia.] |
|
tooth agenesis
|
DOID_0050591 |
[A tooth disease characterized by failure to develop one or more missing teeth.] |
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pyoureter
|
DOID_1425 |
|
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obsolete Mycobacterium infectious disease
|
DOID_2757 |
|
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intestinal schistosomiasis
|
DOID_0050597 |
[A schistosomiasis that involves parasitic infection of the intestine caused by Schistosoma mansoni, Schistosoma intercalatum or Schistosomiasis japonicum. The symptoms include fever, cough, abdominal pain, diarrhea, hepatosplenomegaly, colonic polyposis with bloody diarrhea and eosinophilia.] |
|
type 1 diabetes mellitus 5
|
DOID_0110744 |
[A type 1 diabetes mellitus that has_material_basis_in mutation of the SUMO4 gene on chromosome 6q25.1.] |
|
type 1 diabetes mellitus 6
|
DOID_0110745 |
[A type 1 diabetes mellitus that has_material_basis_in mutation of the locus at chromosome 18q21.] |
|
type 1 diabetes mellitus 3
|
DOID_0110742 |
[A type 1 diabetes mellitus that has_material_basis_in mutation of the locus at chromosome 15q26.] |
|
type 1 diabetes mellitus 4
|
DOID_0110743 |
[A type 1 diabetes mellitus that has_material_basis_in mutation of the locus at chromosome 11q13.] |
|
neurodegeneration with brain iron accumulation 6
|
DOID_0110740 |
[A neurodegeneration with brain iron accumulation that has_material_basis_in autosomal recessive inheritance of mutation in the COASY gene on chromosome 17q21.2.] |
|
neurodegeneration with brain iron accumulation
|
DOID_0110734 |
[A neurodegenerative disease characterized by progressive iron accumulation in the basal ganglia and other regions of the brain, resulting in extrapyramidal movements, such as parkinsonism and dystonia.] |
|
type 1 diabetes mellitus 2
|
DOID_0110741 |
[A type 1 diabetes mellitus that has_material_basis_in autosomal dominant inheritance of mutation of the INS gene on chromosome 11p15.5.] |
|
air pollution
|
OMIT_0001823 |
[A chemical driver that is air pollution, that is composed of a mixture of chemical and particulate matter pollutants in outdoor air, including but not limited to carbon monoxide, ozone, sulfur dixoide, nitrogen dioxide, lead, and fine partiuculate matter. Vehicle emissions, fuel oils and natural gas to heat homes, by-products of manufacturing and power generation, particularly coal-fueled power plants, and fumes from chemical production are the primary sources of human-made air pollution. A pollution process during which particulates or other contaminants are released into a portion of air.] |
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obsolete type 1 diabetes mellitus 9
|
DOID_0110748 |
|
|
type 1 diabetes mellitus 10
|
DOID_0110749 |
[A type 1 diabetes mellitus that has_material_basis_in mutation of the IL2RA gene on chromosome 10p15.1.] |
|
type 1 diabetes mellitus 7
|
DOID_0110746 |
[A type 1 diabetes mellitus that has_material_basis_in mutation of the locus at chromosome 2q31.] |
|
type 1 diabetes mellitus 8
|
DOID_0110747 |
[A type 1 diabetes mellituss that has_material_basis_in mutation of the locus at chromosome 6q25-q27.] |
|
dentin sensitivity
|
DOID_698 |
|
|
glycogen storage disease IV
|
DOID_2750 |
[A glycogen storage disease that has_material_basis_in homozygous or compound heterozygous mutation in the GBE1 gene, which encodes the glycogen branching enzyme, on chromosome 3p12.] |