From HPO
Abnormality of the cardiovascular system- MedGen UID:
- 116727
- •Concept ID:
- C0243050
- •
- Congenital Abnormality
Any abnormality of the cardiovascular system.
Vomiting- MedGen UID:
- 12124
- •Concept ID:
- C0042963
- •
- Sign or Symptom
Forceful ejection of the contents of the stomach through the mouth by means of a series of involuntary spasmic contractions.
Feeding difficulties in infancy- MedGen UID:
- 436211
- •Concept ID:
- C2674608
- •
- Finding
Impaired feeding performance of an infant as manifested by difficulties such as weak and ineffective sucking, brief bursts of sucking, and falling asleep during sucking. There may be difficulties with chewing or maintaining attention.
Seizure- MedGen UID:
- 20693
- •Concept ID:
- C0036572
- •
- Sign or Symptom
A seizure is an intermittent abnormality of nervous system physiology characterized by a transient occurrence of signs and/or symptoms due to abnormal excessive or synchronous neuronal activity in the brain.
Apnea- MedGen UID:
- 2009
- •Concept ID:
- C0003578
- •
- Sign or Symptom
Lack of breathing with no movement of the respiratory muscles and no exchange of air in the lungs. This term refers to a disposition to have recurrent episodes of apnea rather than to a single event.
Hyperkalemia- MedGen UID:
- 5691
- •Concept ID:
- C0020461
- •
- Finding
An abnormally increased potassium concentration in the blood.
Hypoglycemia- MedGen UID:
- 6979
- •Concept ID:
- C0020615
- •
- Disease or Syndrome
A decreased concentration of glucose in the blood.
Hyponatremia- MedGen UID:
- 6984
- •Concept ID:
- C0020625
- •
- Finding
An abnormally decreased sodium concentration in the blood.
Cyanosis- MedGen UID:
- 1189
- •Concept ID:
- C0010520
- •
- Sign or Symptom
Bluish discoloration of the skin and mucosa due to poor circulation or inadequate oxygenation of arterial or capillary blood.
Abnormality of skin pigmentation- MedGen UID:
- 224697
- •Concept ID:
- C1260926
- •
- Finding
An abnormality of the pigmentation of the skin.
Adrenal insufficiency- MedGen UID:
- 1351
- •Concept ID:
- C0001623
- •
- Disease or Syndrome
Insufficient production of steroid hormones (primarily cortisol) by the adrenal glands.
Adrenal hypoplasia- MedGen UID:
- 337539
- •Concept ID:
- C1846223
- •
- Pathologic Function
Developmental hypoplasia of the adrenal glands.
- Abnormality of metabolism/homeostasis
- Abnormality of the cardiovascular system
- Abnormality of the digestive system
- Abnormality of the endocrine system
- Abnormality of the integument
- Abnormality of the nervous system
- Abnormality of the respiratory system