|
obsolete Sezary's disease involving spleen
|
DOID_8626 |
|
|
hypoplastic left heart syndrome
|
DOID_9955 |
[A congenital heart disease characterized by abnormal development of the left-sided structures of the heart.] |
|
obsolete adhesions and disruptions of pupillary membranes
|
DOID_8623 |
|
|
null-cell leukemia
|
DOID_9954 |
|
|
male breast
|
UBERON_0016410 |
|
|
obsolete Hodgkin's lymphoma, lymphocytic depletion, involving lymph nodes of inguinal region and lower limb
|
DOID_8627 |
|
|
Hodgkin's lymphoma, lymphocytic depletion
|
DOID_8628 |
|
|
hemometra
|
DOID_9958 |
[A uterine disease that is characterized by the presence of blood in the uterine cavity.] |
|
secondary corneal edema
|
DOID_11032 |
|
|
corneal edema
|
DOID_11030 |
|
|
obsolete bilateral vesicoureteral reflux with reflux nephropathy
|
DOID_13695 |
|
|
pulsating exophthalmos
|
DOID_12364 |
|
|
asphyxiating thoracic dystrophy 3
|
DOID_0110087 |
[An asphyxiating thoracic dystrophy that has_material_basis_in homozygous or compound heterozygous mutation in the DYNC2H1 gene on chromosome 11q22.] |
|
intermittent proptosis
|
DOID_12363 |
|
|
obsolete unilateral vesicoureteral reflux with reflux nephropathy
|
DOID_13694 |
|
|
idiopathic corneal edema
|
DOID_11033 |
|
|
asphyxiating thoracic dystrophy 4
|
DOID_0110088 |
[An asphyxiating thoracic dystrophy has_material_basis_in compound heterozygous mutation in the TTC21B gene on chromosome 2q24.] |
|
thyrotoxic exophthalmos
|
DOID_12362 |
|
|
obsolete disorder of ureter
|
DOID_13693 |
|
|
asphyxiating thoracic dystrophy 1
|
DOID_0110085 |
[An asphyxiating thoracic dystrophy associated with variation in the region 15q13.] |
