From HPO
Neurogenic bladder- MedGen UID:
- 595
- •Concept ID:
- C0005697
- •
- Disease or Syndrome
A type of bladder dysfunction caused by neurologic damage. Neurogenic bladder can be flaccid or spastic. Common manifestatios of neurogenic bladder are overflow incontinence, frequency, urgency, urge incontinence, and retention.
Dextrocardia- MedGen UID:
- 4255
- •Concept ID:
- C0011813
- •
- Congenital Abnormality
The heart is located in the right hand sided hemithorax. That is, there is a left-right reversal (or "mirror reflection") of the anatomical location of the heart in which the heart is locate on the right side instead of the left.
Vertebral artery hypoplasia- MedGen UID:
- 833617
- •Concept ID:
- C1868737
- •
- Disease or Syndrome
Underdevelopment of the vertebral artery.
Unilateral vertebral artery hypoplasia- MedGen UID:
- 480720
- •Concept ID:
- C3279090
- •
- Finding
Underdevelopment of the vertebral artery on one side.
Situs inversus- MedGen UID:
- 1642262
- •Concept ID:
- C4551493
- •
- Congenital Abnormality
A left-right reversal (or "mirror reflection") of the anatomical location of the major thoracic and abdominal organs.
Aplasia of posterior communicating artery- MedGen UID:
- 1841851
- •Concept ID:
- C5826484
- •
- Congenital Abnormality
A developmental anomnaly characterized by the lack of development of the posterior communicating artery.
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).
Anal stenosis- MedGen UID:
- 82644
- •Concept ID:
- C0262374
- •
- Anatomical Abnormality
Abnormal narrowing of the anal opening.
Ectopic anus- MedGen UID:
- 75606
- •Concept ID:
- C0266231
- •
- Congenital Abnormality
Abnormal displacement or malposition of the anus.
Hydrocephalus- MedGen UID:
- 9335
- •Concept ID:
- C0020255
- •
- Disease or Syndrome
Hydrocephalus is an active distension of the ventricular system of the brain resulting from inadequate passage of CSF from its point of production within the cerebral ventricles to its point of absorption into the systemic circulation.
Myelomeningocele- MedGen UID:
- 7538
- •Concept ID:
- C0025312
- •
- Congenital Abnormality
Protrusion of the meninges and portions of the spinal cord through a defect of the vertebral column.
Spina bifida occulta- MedGen UID:
- 36380
- •Concept ID:
- C0080174
- •
- Congenital Abnormality
The closed form of spina bifida with incomplete closure of a vertebral body with intact overlying skin.
Chiari type II malformation- MedGen UID:
- 108222
- •Concept ID:
- C0555206
- •
- Congenital Abnormality
Chiari malformation type II (CM2), also known as the Arnold-Chiari malformation, consists of elongation and descent of the inferior cerebellar vermis, cerebellar hemispheres, pons, medulla, and fourth ventricle through the foramen magnum into the spinal canal. CM2 is uniquely associated with myelomeningocele (open spina bifida; see 182940) and is found only in this population (Stevenson, 2004). It is believed to be a disorder of neuroectodermal origin (Schijman, 2004).
For a general phenotypic description of the different forms of Chiari malformations, see Chiari malformation type I (CM1; 118420).
Scoliosis- MedGen UID:
- 11348
- •Concept ID:
- C0036439
- •
- Disease or Syndrome
The presence of an abnormal lateral curvature of the spine.
Hemivertebrae- MedGen UID:
- 82720
- •Concept ID:
- C0265677
- •
- Congenital Abnormality
Absence of one half of the vertebral body.
Rib fusion- MedGen UID:
- 78570
- •Concept ID:
- C0265695
- •
- Congenital Abnormality
Complete or partial merging of adjacent ribs.
Short thorax- MedGen UID:
- 140876
- •Concept ID:
- C0426789
- •
- Finding
Reduced inferior to superior extent of the thorax.
Missing ribs- MedGen UID:
- 98093
- •Concept ID:
- C0426816
- •
- Finding
A developmental anomaly with absence of one or more ribs.
Vertebral segmentation defect- MedGen UID:
- 96577
- •Concept ID:
- C0432163
- •
- Congenital Abnormality
An abnormality related to a defect of vertebral separation during development.
Block vertebrae- MedGen UID:
- 375498
- •Concept ID:
- C1844753
- •
- Congenital Abnormality
Congenital synostosis between two or more adjacent vertebrae (partial or complete fusion of adjacent vertabral bodies).
Abnormal odontoid process morphology- MedGen UID:
- 351218
- •Concept ID:
- C1864794
- •
- Anatomical Abnormality
Abnormal structure of the odontoid process, which is a part of the C2 or axis vertebra and forms pivot of the structures forming the craniovertebral junction. The odontoid process is also known as the dens of the axis.
Bell-shaped thorax- MedGen UID:
- 351320
- •Concept ID:
- C1865186
- •
- Finding
The rib cage has the shape of a wide mouthed bell. That is, the superior portion of the rib cage is constricted, followed by a convex region, and the inferior portion of the rib cage expands again to have a large diameter.
Pectus excavatum- MedGen UID:
- 781174
- •Concept ID:
- C2051831
- •
- Finding
A defect of the chest wall characterized by a depression of the sternum, giving the chest ("pectus") a caved-in ("excavatum") appearance.
Vertebral fusion- MedGen UID:
- 480139
- •Concept ID:
- C3278509
- •
- Anatomical Abnormality
A developmental defect leading to the union of two adjacent vertebrae.
Reduced forced vital capacity- MedGen UID:
- 337630
- •Concept ID:
- C1846678
- •
- Finding
An abnormal reduction in the amount of air a person can expel following maximal inspiration.
Restrictive ventilatory defect- MedGen UID:
- 478856
- •Concept ID:
- C3277226
- •
- Finding
A functional defect characterized by reduced total lung capacity (TLC) not associated with abnormalities of expiratory airflow or airway resistance. Spirometrically, a restrictive defect is defined as FEV1 (forced expiratory volume in 1 second) and FVC (forced vital capacity) less than 80 per cent. Restrictive lung disease may be caused by alterations in lung parenchyma or because of a disease of the pleura, chest wall, or neuromuscular apparatus.
Reduced forced expiratory volume in one second- MedGen UID:
- 1687063
- •Concept ID:
- C5139283
- •
- Finding
An abnormal reduction in the amount of air a person can forcefully expel in one second.
Short neck- MedGen UID:
- 99267
- •Concept ID:
- C0521525
- •
- Finding
Diminished length of the neck.
Broad neck- MedGen UID:
- 344099
- •Concept ID:
- C1853638
- •
- Finding
Increased side-to-side width of the neck.
- Abnormality of head or neck
- Abnormality of the cardiovascular system
- Abnormality of the digestive system
- Abnormality of the genitourinary system
- Abnormality of the musculoskeletal system
- Abnormality of the nervous system
- Abnormality of the respiratory system
- Growth abnormality