|
sarcoid meningitis
|
DOID_12055 |
|
|
Fanconi anemia complementation group D1
|
DOID_0111089 |
[A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the BRCA2 gene on chromosome 13q13.] |
|
obsolete Trypanosoma meningitis
|
DOID_12054 |
[A trypanosomiasis that involves inflammation of the meninges caused due to Trypanosoma species.] |
|
Fanconi anemia complementation group G
|
DOID_0111086 |
[A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the XRCC9 gene on chromosome 9p13.] |
|
cryptococcosis
|
DOID_12053 |
[An opportunistic mycosis that results_in fungal infection and has_material_basis_in Cryptococcus neoformans or Cryptococcus gattii.] |
|
Fanconi anemia complementation group C
|
DOID_0111087 |
[A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCC gene on chromosome 9q22.] |
|
obsolete cryptococcal meningitis
|
DOID_12052 |
[A cryptococcosis that results_in inflammation located_in meninges, has_material_basis_in Cryptococcus neoformans and has_symptom headache, has_symptom nausea, has_symptom staggering gait, has_symptom dementia, has_symptom blurred vision and has_symptom confusion.] |
|
Fanconi anemia complementation group E
|
DOID_0111084 |
[A Fanconi anemia that has_material_basis_in homozygous mutation in the FANCE gene on chromosome 6p22-p21.] |
|
megaloblastic anemia
|
DOID_13382 |
[A macrocytic anemia that is characterized by inhibition of DNA synthesis during red blood cell production.] |
|
Fanconi anemia complementation group U
|
DOID_0111085 |
[A Fanconi anemia that has_material_basis_in homozygous mutation in the XRCC2 gene on chromosome 7q36.] |
|
pernicious anemia
|
DOID_13381 |
[A nutritional deficiency disease that is characterized by a decrease in red blood cells due to malabsorption of vitamin B12, has_symptom fatigue, pallor, shortness of breath, glossitis, ataxia, and/or paresthesia, has_material_basis_in atrophic gastritis, autoimmune disorder affecting the production or function of intrinsic factor, and/or genetic factors.] |
|
Fanconi anemia complementation group L
|
DOID_0111082 |
[A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the PHF9 gene on chromosome 2p16.] |
|
obsolete acute pyelonephritis with lesion of renal medullary necrosis
|
DOID_13380 |
|
|
Fanconi anemia complementation group D2
|
DOID_0111083 |
[A Fanconi anemia that has_material_basis_in compound heterozygous or homozygous mutation in the FANCD2 gene on chromosome 3p25.] |
|
Oligoryzomys longicaudatus
|
NCBITaxon_137207 |
|
|
Oligoryzomys
|
NCBITaxon_29120 |
|
|
obsolete Fetal-maternal hemorrhage affecting management of mother
|
DOID_12058 |
|
|
labia majora carcinoma
|
DOID_13389 |
[A vulva carcinoma that is located_in the labia majora.] |
|
Fanconi anemia complementation group I
|
DOID_0111091 |
[A Fanconi anemia that has_material_basis_in homozygous or compound heterozygous mutation in the FANCI gene on chromosome 15q26.] |
|
Fanconi anemia complementation group P
|
DOID_0111092 |
[A Fanconi anemia characterized by increased chromosomal instability, progressive bone marrow failure and in some cases skeletal abnormalities that has_material_basis_in homozygous or compound heterozygous mutation in the SLX4 gene on chromosome 16p13.3.] |