|
perforation of bile duct
|
DOID_13409 |
|
|
obsolete metastasis to pleura
|
DOID_13408 |
|
|
hypercalcemic sarcoidosis
|
DOID_13407 |
|
|
obsolete progressive high-tone neural deafness
|
DOID_14739 |
|
|
trichorhinophalangeal syndrome type I
|
DOID_14743 |
[A syndrome that is characterized by short stature, sparse hair, a bulbous nasal tip and cone-shaped epiphyses (the growing ends of bones), as well as severe generalized shortening of all finger and toe bones (brachydactyly).] |
|
Partington syndrome
|
DOID_14744 |
[A syndrome characterized by intellectual disability, focal dystonia of the hands and dysarthria.] |
|
alexia
|
DOID_13417 |
[An agnosia that is a loss of the ability to recognize text.] |
|
obsolete diabetes mellitus insulin dependent type, not stated as uncontrolled, with peripheral circulatory disorder
|
DOID_13416 |
|
|
hepatic encephalopathy
|
DOID_13413 |
[A brain disease that is characterized by loss of brain function, the occurrence of confusion, altered level of consciousness, and coma that results when the liver is unable to remove toxins from the blood.] |
|
neurogenic bowel
|
DOID_13419 |
|
|
isovaleric acidemia
|
DOID_14753 |
[An organic acidemia that disrupts or prevents normal metabolism of the branched-chain amino acid leucine.] |
|
argininosuccinic aciduria
|
DOID_14755 |
[An amino acid metabolic disorder that involves the accumulation of argininosuccinic acid (ASA) in the blood and urine.] |
|
Crotonoideae
|
NCBITaxon_235631 |
|
|
vascular type Ehlers-Danlos syndrome
|
DOID_14756 |
[An Ehlers-Danlos syndrome that has_material_basis_in heterozygous mutation in the COL3A1 gene on chromosome 2q32 and that is characterized by the association of unexpected organ fragility (arterial/bowel/gravid uterine rupture) with inconstant physical features as thin, translucent skin, easy bruising and acrogeric traits.] |
|
Ehlers-Danlos syndrome hypermobility type
|
DOID_14757 |
[An Ehlers-Danlos syndrome that is characterized by joint hyperextensibility without skeletal deformity.] |
|
autosomal recessive type IV Ehlers-Danlos syndrome
|
DOID_14759 |
[An Ehlers-Danlos syndrome that is characterized by the association of unexpected organ fragility (arterial/bowel/gravid uterine rupture) with inconstant physical features as thin, translucent skin, easy bruising and acrogeric traits.] |
|
Digenea <flatworms>
|
NCBITaxon_6179 |
|
|
susceptibility to follicular lymphoma 1
|
MIM_613024 |
|
|
diphtheritic peritonitis
|
DOID_13310 |
[A peritonitis which involves inflammation of peritoneal cavity by Corynebacterium diphtheriae.] |
|
African iron overload
|
DOID_0111033 |
[A hemochromatosis characterized by a predisposition to iron loading that is exacerbated by excessive intake of dietary iron, commonly related to consumption of tradition beer brewed in non-galvanized steel drums.] |