|
psoriasis 3
|
DOID_0111283 |
[A psoriasis that has_material_basis_in variation in a region on chromosome 4q.] |
|
psoriasis 4
|
DOID_0111280 |
[A psoriasis that has_material_basis_in variation in a region on chromosome 1q21.] |
|
electrically active cell
|
CL_0000211 |
|
|
psoriasis 15
|
DOID_0111281 |
[A psoriasis characterized by pustular psoriasis that has_material_basis_in heterozygous mutation in the AP1S3 gene on chromosome 2q36.1.] |
|
hemophilia B
|
DOID_12259 |
[A hemophilia that has_material_basis_in Factor IX deficiency, which makes coagulation much more prolonged. The disease is inherited as an X-linked recessive trait.] |
|
female infertility of uterine origin
|
DOID_13589 |
[A uterine disease that is characterized by an inability to get pregnant despite having carefully timed, unprotected sex for one year.] |
|
obsolete acquired factor IX deficiency
|
DOID_12258 |
|
|
medulloadrenal hyperfunction
|
DOID_12257 |
|
|
obsolete adrenogenital disease
|
DOID_12256 |
|
|
psoriasis 8
|
DOID_0111288 |
[A psoriasis that has_material_basis_in variation in a region on chromosome 16q. This region overlaps one that is associated with inflammatory bowel disease 1 disease.] |
|
obsolete congenital adrenal hyperplasia
|
DOID_12255 |
|
|
psoriasis 10
|
DOID_0111289 |
[A psoriasis that has_material_basis_in variation in a region on chromosome 18p11.23.] |
|
polyarteritis nodosa
|
DOID_9810 |
[A vasculitis that is characterized by necrotizing inflammation of medium or small arteries.] |
|
psoriasis 6
|
DOID_0111290 |
[A psoriasis that has_material_basis_in variation in a region on chromosome 19p13 that includes BSG.] |
|
Sertoli cell
|
CL_0000216 |
|
|
seminiferous tubule epithelial cell
|
CL_0002625 |
|
|
partial circumpapillary choroid dystrophy
|
DOID_9811 |
|
|
obsolete retinal defect
|
DOID_9818 |
|
|
obsolete partial recent retinal detachment with giant tear
|
DOID_9816 |
|
|
obsolete Recent retinal detachment, total or subtotal
|
DOID_9815 |
|