From HPO
Red urine- MedGen UID:
- 910906
- •Concept ID:
- C0858862
- •
- Finding
An abnormal red color of the urine.
Pink urine- MedGen UID:
- 376643
- •Concept ID:
- C1849715
- •
- Finding
An abnormal pink color of urine.
Short stature- MedGen UID:
- 87607
- •Concept ID:
- C0349588
- •
- Finding
A height below that which is expected according to age and gender norms. Although there is no universally accepted definition of short stature, many refer to "short stature" as height more than 2 standard deviations below the mean for age and gender (or below the 3rd percentile for age and gender dependent norms).
Cholelithiasis- MedGen UID:
- 3039
- •Concept ID:
- C0008350
- •
- Disease or Syndrome
Hard, pebble-like deposits that form within the gallbladder.
Hepatomegaly- MedGen UID:
- 42428
- •Concept ID:
- C0019209
- •
- Finding
Abnormally increased size of the liver.
Jaundice- MedGen UID:
- 43987
- •Concept ID:
- C0022346
- •
- Sign or Symptom
Yellow pigmentation of the skin due to bilirubin, which in turn is the result of increased bilirubin concentration in the bloodstream.
Increased fecal coproporphyrin 1- MedGen UID:
- 1719205
- •Concept ID:
- C5397995
- •
- Finding
Abnormally high concentration of coproporphyrin 1 in feces.
Hemolytic anemia- MedGen UID:
- 1916
- •Concept ID:
- C0002878
- •
- Disease or Syndrome
A type of anemia caused by premature destruction of red blood cells (hemolysis).
Thrombocytopenia- MedGen UID:
- 52737
- •Concept ID:
- C0040034
- •
- Disease or Syndrome
A reduction in the number of circulating thrombocytes.
Pathologic fracture- MedGen UID:
- 42095
- •Concept ID:
- C0016663
- •
- Pathologic Function
A pathologic fracture occurs when a bone breaks in an area that is weakened secondarily to another disease process such as tumor, infection, and certain inherited bone disorders. A pathologic fracture can occur without a degree of trauma required to cause fracture in healthy bone.
Osteopenia- MedGen UID:
- 18222
- •Concept ID:
- C0029453
- •
- Disease or Syndrome
Osteopenia is a term to define bone density that is not normal but also not as low as osteoporosis. By definition from the World Health Organization osteopenia is defined by bone densitometry as a T score -1 to -2.5.
Joint contracture of the hand- MedGen UID:
- 56382
- •Concept ID:
- C0158113
- •
- Finding
Contractures of one ore more joints of the hands meaning chronic loss of joint motion due to structural changes in non-bony tissue.
Vertebral compression fracture- MedGen UID:
- 75497
- •Concept ID:
- C0262431
- •
- Finding
Corneal scarring- MedGen UID:
- 83899
- •Concept ID:
- C0349702
- •
- Finding
Replacement of corneal tissue with scar tissue as a result of injury to the deeper layers of the cornea.
Atypical scarring of skin- MedGen UID:
- 867415
- •Concept ID:
- C4021786
- •
- Pathologic Function
Atypically scarred skin .
Osteolysis- MedGen UID:
- 1648424
- •Concept ID:
- C4721411
- •
- Pathologic Function
Osteolysis refers to the destruction of bone through bone resorption with removal or loss of calcium.
Conjunctivitis- MedGen UID:
- 1093
- •Concept ID:
- C0009763
- •
- Disease or Syndrome
Inflammation of the conjunctiva.
Splenomegaly- MedGen UID:
- 52469
- •Concept ID:
- C0038002
- •
- Finding
Abnormal increased size of the spleen.
Elevated circulating uroporphyrin concentration- MedGen UID:
- 1842099
- •Concept ID:
- C5826755
- •
- Finding
Concentration of uroporphyrin in the blood circulation above the upper limit of normal.
Reduced erythrocyte uroporphyrinogen III cosynthase activity- MedGen UID:
- 1054010
- •Concept ID:
- CN377345
- •
- Finding
Activity or concentration of in the level of uroporphyrinogen III (EC 4.2.1.75) in erythrocytes below the lower limit of normal.
Absent eyebrow- MedGen UID:
- 98133
- •Concept ID:
- C0431448
- •
- Congenital Abnormality
Absence of the eyebrow.
Erythrodontia- MedGen UID:
- 901544
- •Concept ID:
- C4280783
- •
- Finding
Reddish, brown opalescent discoloration of teeth in normal light.
Alopecia- MedGen UID:
- 7982
- •Concept ID:
- C0002170
- •
- Finding
A noncongenital process of hair loss, which may progress to partial or complete baldness.
Scleroderma- MedGen UID:
- 3770
- •Concept ID:
- C0011644
- •
- Disease or Syndrome
A chronic autoimmune phenomenon characterized by fibrosis (or hardening) and vascular alterations of the skin.
Hypertrichosis- MedGen UID:
- 43787
- •Concept ID:
- C0020555
- •
- Disease or Syndrome
Hypertrichosis is increased hair growth that is abnormal in quantity or location.
Hyperpigmentation of the skin- MedGen UID:
- 57992
- •Concept ID:
- C0162834
- •
- Pathologic Function
A darkening of the skin related to an increase in melanin production and deposition.
Hypopigmentation of the skin- MedGen UID:
- 102477
- •Concept ID:
- C0162835
- •
- Disease or Syndrome
A reduction of skin color related to a decrease in melanin production and deposition.
Thickened skin- MedGen UID:
- 66024
- •Concept ID:
- C0241165
- •
- Finding
Laminar thickening of skin.
Cutaneous photosensitivity- MedGen UID:
- 87601
- •Concept ID:
- C0349506
- •
- Pathologic Function
An increased sensitivity of the skin to light. Photosensitivity may result in a rash upon exposure to the sun (which is known as photodermatosis). Photosensitivity can be diagnosed by phototests in which light is shone on small areas of skin.
Loss of eyelashes- MedGen UID:
- 1390509
- •Concept ID:
- C4316878
- •
- Finding
This term refers to the loss of eyelashes that were previously present.
- Abnormality of blood and blood-forming tissues
- Abnormality of head or neck
- Abnormality of metabolism/homeostasis
- Abnormality of the digestive system
- Abnormality of the genitourinary system
- Abnormality of the immune system
- Abnormality of the integument
- Abnormality of the musculoskeletal system
- Growth abnormality