From HPO
Primary testicular failure- MedGen UID:
- 235162
- •Concept ID:
- C1384582
- •
- Disease or Syndrome
Testicular failure due to a condition directly affecting the testes.
Atrial fibrillation- MedGen UID:
- 445
- •Concept ID:
- C0004238
- •
- Finding
An atrial arrhythmia characterized by disorganized atrial activity without discrete P waves on the surface EKG, but instead by an undulating baseline or more sharply circumscribed atrial deflections of varying amplitude an frequency ranging from 350 to 600 per minute.
Congestive heart failure- MedGen UID:
- 9169
- •Concept ID:
- C0018802
- •
- Disease or Syndrome
The presence of an abnormality of cardiac function that is responsible for the failure of the heart to pump blood at a rate that is commensurate with the needs of the tissues or a state in which abnormally elevated filling pressures are required for the heart to do so. Heart failure is frequently related to a defect in myocardial contraction.
Tricuspid regurgitation- MedGen UID:
- 11911
- •Concept ID:
- C0040961
- •
- Disease or Syndrome
Failure of the tricuspid valve to close sufficiently upon contraction of the right ventricle, causing blood to regurgitate (flow backward) into the right atrium.
Vasculitis- MedGen UID:
- 12054
- •Concept ID:
- C0042384
- •
- Disease or Syndrome
Inflammation of blood vessel.
Cardiomyopathy- MedGen UID:
- 209232
- •Concept ID:
- C0878544
- •
- Disease or Syndrome
A myocardial disorder in which the heart muscle is structurally and functionally abnormal, in the absence of coronary artery disease, hypertension, valvular disease and congenital heart disease sufficient to cause the observed myocardial abnormality.
Right ventricular cardiomyopathy- MedGen UID:
- 384481
- •Concept ID:
- C2063326
- •
- Disease or Syndrome
Right ventricular dysfunction (global or regional) with functional and morphological right ventricular abnormalities, with or without left ventricular disease.
Sensorineural hearing loss disorder- MedGen UID:
- 9164
- •Concept ID:
- C0018784
- •
- Disease or Syndrome
A type of hearing impairment in one or both ears related to an abnormal functionality of the cochlear nerve.
Congenital posterior occipital alopecia- MedGen UID:
- 870405
- •Concept ID:
- C4024850
- •
- Congenital Abnormality
Loss of hair in the occipital region of the scalp with congenital onset.
Collagenoma- MedGen UID:
- 1053829
- •Concept ID:
- CN376537
- •
- Finding
A rare hamartomatous malformation characterized by the predominant proliferation of normal collagen fibers and normal, decreased, or increased elastic fibers. Collagenomas may be solitary or multiple, sporadic, acquired or inherited.
Iris atrophy- MedGen UID:
- 96095
- •Concept ID:
- C0423319
- •
- Disease or Syndrome
Loss of iris tissue (atrophy)
- Abnormality of the cardiovascular system
- Abnormality of the eye
- Abnormality of the genitourinary system
- Abnormality of the integument
- Ear malformation