|
right lower quadrant pelvic lump
|
SYMP_0000775 |
|
|
pelvic mass
|
SYMP_0000772 |
|
|
pelvic symptom
|
SYMP_0000770 |
|
|
obsolete Hodgkin's lymphoma, lymphocytic depletion, involving intrathoracic lymph nodes
|
DOID_8854 |
|
|
developmental and epileptic encephalopathy 3
|
DOID_0080440 |
[A developmental and epileptic encephalopathy characterized by onset in the first months of life of erratic, typically myoclonic, refractory seizures that has_material_basis_in homozygous or compound heterozygous mutation in the SLC25A22 gene on chromosome 11p15.] |
|
pelvic swelling
|
SYMP_0000771 |
|
|
acute gonococcal endometritis
|
DOID_7527 |
[An acute endometritis that is caused by gonorrhea.] |
|
acute endometritis
|
DOID_7528 |
[An endometritis that is characterized by onset within the past 1 - 3 days.] |
|
developmental and epileptic encephalopathy 46
|
DOID_0080456 |
[A developmental and epileptic encephalopathy characterized by onset in the first months or years of life of intractable seizures, global developmental delay, failure to thrive, hypotonia, hyperreflexia, and variably impaired intellectual development that has_material_basis_in heterozygous mutation in the GRIN2D gene on chromosome 19q13.] |
|
microcephaly, seizures, and developmental delay
|
DOID_0080457 |
[A developmental and epileptic encephalopathy characterized by microcephaly, infantile onset of seizures and developmental delay that has_material_basis_in homozygous or compound heterozygous mutation in the PNKP gene on chromosome 19q13.] |
|
developmental and epileptic encephalopathy 35
|
DOID_0080458 |
[A developmental and epileptic encephalopathy characterized by seizure onset in the first months of life, absence of normal development and absence of myelination of early neurological structures that has_material_basis_in homozygous or compound heterozygous mutation in the ITPA gene on chromosome 20p13.] |
|
developmental and epileptic encephalopathy 12
|
DOID_0080459 |
[A developmental and epileptic encephalopathy characterized by onset of refractory seizures in the first year of life with normal to mild developmental delay before onset of seizures but developmental regression and stagnation after seizure onset that has_material_basis_in homozygous or compound heterozygous mutation in the PLCB1 gene on chromosome 20p12.3.] |
|
right lower quadrant pelvic mass
|
SYMP_0000789 |
|
|
developmental and epileptic encephalopathy 28
|
DOID_0080452 |
[A developmental and epileptic encephalopathy characterized by onset in the first months of life of refractory seizures, severe axial hypotonia, and profoundly impaired psychomotor development that has_material_basis_in homozygous or compound heterozygous mutation in the WWOX gene on chromosome 16q23.] |
|
developmental and epileptic encephalopathy 25
|
DOID_0080453 |
[A developmental and epileptic encephalopathy characterized by onset in early infancy of refractory seizures, global developmental delay with intellectual disability, persistent neurologic symptoms, and dental anomalies that has_material_basis_in homozygous or compound heterozygous mutation in the SLC13A5 gene on chromosome 17p13.] |
|
periumbilic pelvic mass
|
SYMP_0000787 |
|
|
developmental and epileptic encephalopathy 42
|
DOID_0080454 |
[A developmental and epileptic encephalopathy characterized by onset of seizures in the first hours or days of life and global developmental delay with severely impaired intellectual development that has_material_basis_in heterozygous mutation in the CACNA1A gene on chromosome 19p13.] |
|
multiple sites pelvic mass
|
SYMP_0000788 |
|
|
developmental and epileptic encephalopathy 52
|
DOID_0080455 |
[A developmental and epileptic encephalopathy characterized by infantile onset of refractory seizures and global neurological development delay, and intellectual disability that has_material_basis_in homozygous or compound heterozygous mutation in the SCN1B gene on chromosome 19q13.] |
|
obsolete lymphosarcoma involving spleen
|
DOID_8860 |
|
