|
thiopental
|
CHEBI_102166 |
|
|
barbiturates
|
CHEBI_22693 |
|
|
hypospadias
|
DOID_10892 |
[A physical disorder characterized by an abnormally placed urethral opening on the underside of the penis or on the perineum.] |
|
nuclear complex of neuraxis
|
UBERON_0007245 |
|
|
gray matter
|
UBERON_0002020 |
|
|
finger
|
UBERON_0002389 |
|
|
Xenopsylla
|
NCBITaxon_163158 |
|
|
Xenopsyllinae
|
NCBITaxon_476427 |
|
|
Xenopsylla cheopis
|
NCBITaxon_163159 |
|
|
nuclear type mitochondrial complex I deficiency 11
|
DOID_0112089 |
[A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFAF1 gene on chromosome 15q15.1.] |
|
nuclear type mitochondrial complex I deficiency
|
DOID_0112065 |
[A mitochondrial complex I deficiency that has_material_basis_in mutation in a gene in the nuclear genome.] |
|
nuclear type mitochondrial complex I deficiency 21
|
DOID_0112088 |
[A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NUBPL gene on chromosome 14q12.] |
|
nuclear type mitochondrial complex I deficiency 23
|
DOID_0112087 |
[A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA12 gene on chromosome 12q22.] |
|
nuclear type mitochondrial complex I deficiency 26
|
DOID_0112086 |
[A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFA9 gene on chromosome 12p13.32.] |
|
nuclear type mitochondrial complex I deficiency 19
|
DOID_0112085 |
[A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the FOXRED1 gene on chromosome 11q24.2.] |
|
nuclear type mitochondrial complex I deficiency 29
|
DOID_0112084 |
[A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the TMEM126B gene on chromosome 11q14.1.] |
|
nuclear type mitochondrial complex I deficiency 2
|
DOID_0112083 |
[A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFS8 gene on chromosome 11q13.2.] |
|
obsolete metastatic squamous cell carcinoma
|
DOID_4099 |
|
|
nuclear type mitochondrial complex I deficiency 3
|
DOID_0112093 |
[A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFS7 gene on chromosome 19p13.3.] |
|
nuclear type mitochondrial complex I deficiency 7
|
DOID_0112092 |
[A nuclear type mitochondrial complex I deficiency that has_material_basis_in homozygous or compound heterozygous mutation in the NDUFV2 gene on chromosome 18p11.22.] |
