From HPO
Nocturia- MedGen UID:
- 14440
- •Concept ID:
- C0028734
- •
- Disease or Syndrome
Abnormally increased production of urine during the night leading to an unusually frequent need to urinate.
Retrograde ejaculation- MedGen UID:
- 98338
- •Concept ID:
- C0403673
- •
- Pathologic Function
The emission of semen and seminal fluid into the bladder instead of through the penis during orgasm.
Brachydactyly- MedGen UID:
- 67454
- •Concept ID:
- C0221357
- •
- Congenital Abnormality
Digits that appear disproportionately short compared to the hand/foot. The word brachydactyly is used here to describe a series distinct patterns of shortened digits (brachydactyly types A-E). This is the sense used here.
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.
Orthostatic hypotension- MedGen UID:
- 43803
- •Concept ID:
- C0020651
- •
- Disease or Syndrome
A form of hypotension characterized by a sudden fall in blood pressure that occurs when a person assumes a standing position.
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.
Isolated prolactin deficiency- MedGen UID:
- 75758
- •Concept ID:
- C0271586
- •
- Finding
A reduced level of prolactin in the blood circulation. Prolactin is a protein hormone that is secreted by lactotrophs in the anterior pituitary and that stimulates mammary gland development and milk production.
Hyporeflexia- MedGen UID:
- 195967
- •Concept ID:
- C0700078
- •
- Finding
Reduction of neurologic reflexes such as the knee-jerk reaction.
Hypotonia- MedGen UID:
- 10133
- •Concept ID:
- C0026827
- •
- Finding
Hypotonia is an abnormally low muscle tone (the amount of tension or resistance to movement in a muscle). Even when relaxed, muscles have a continuous and passive partial contraction which provides some resistance to passive stretching. Hypotonia thus manifests as diminished resistance to passive stretching. Hypotonia is not the same as muscle weakness, although the two conditions can co-exist.
Weakness of facial musculature- MedGen UID:
- 98103
- •Concept ID:
- C0427055
- •
- Disease or Syndrome
Reduced strength of one or more muscles innervated by the facial nerve (the seventh cranial nerve).
Joint hypermobility- MedGen UID:
- 336793
- •Concept ID:
- C1844820
- •
- Finding
The capability that a joint (or a group of joints) has to move, passively and/or actively, beyond normal limits along physiological axes.
Increased blood urea nitrogen- MedGen UID:
- 760252
- •Concept ID:
- C0151539
- •
- Finding
An increased amount of nitrogen in the form of urea in the blood.
Hypomagnesemia- MedGen UID:
- 57481
- •Concept ID:
- C0151723
- •
- Disease or Syndrome
An abnormally decreased magnesium concentration in the blood.
Neonatal hypoglycemia- MedGen UID:
- 57646
- •Concept ID:
- C0158986
- •
- Finding
Blood glucose concentration below the lower limit of established reference ranges in a newborn.
Intermittent hypothermia- MedGen UID:
- 332504
- •Concept ID:
- C1837639
- •
- Finding
Episodes of reduced body termperature.
Elevated circulating dihydroxyphenylacetic acid concentration- MedGen UID:
- 1054866
- •Concept ID:
- CN376747
- •
- Finding
The concentration of dihydroxyphenylacetic acid in the blood circulation is above the upper limit of normal.
Reduced circulating dopamine beta-hydroxylase activity- MedGen UID:
- 1054214
- •Concept ID:
- CN377388
- •
- Finding
Concentration of Dopamine beta-hydroxylase (DBH; EC 1.14.17.1) in the blood circulation below the lower limit of normal. DBH catalyzes the oxidative hydroxylation of dopamine to norepinephrine.
Nasal congestion- MedGen UID:
- 6523
- •Concept ID:
- C0027424
- •
- Sign or Symptom
Reduced ability to pass air through the nasal cavity often leading to mouth breathing.
High palate- MedGen UID:
- 66814
- •Concept ID:
- C0240635
- •
- Congenital Abnormality
Height of the palate more than 2 SD above the mean (objective) or palatal height at the level of the first permanent molar more than twice the height of the teeth (subjective).
Ptosis- MedGen UID:
- 2287
- •Concept ID:
- C0005745
- •
- Disease or Syndrome
The upper eyelid margin is positioned 3 mm or more lower than usual and covers the superior portion of the iris (objective); or, the upper lid margin obscures at least part of the pupil (subjective).
- Abnormality of head or neck
- Abnormality of limbs
- Abnormality of metabolism/homeostasis
- Abnormality of the cardiovascular system
- Abnormality of the eye
- Abnormality of the genitourinary system
- Abnormality of the musculoskeletal system
- Abnormality of the nervous system