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  • The following terms were not found in MedGen: 5E, yeru, Cyrillicij.
1.

Atelosteogenesis type II

Clinical features of atelosteogenesis type 2 (AO2) include rhizomelic limb shortening with normal-sized skull, hitchhiker thumbs, small chest, protuberant abdomen, cleft palate, and distinctive facial features (midface retrusion, depressed nasal bridge, epicanthus, micrognathia). Other typical findings are ulnar deviation of the fingers, gap between the first and second toes, and clubfoot. AO2 is usually lethal at birth or shortly thereafter due to pulmonary hypoplasia and tracheobronchomalacia. However, it exists in a continuous phenotypic spectrum with diastrophic dysplasia, and long-term survivors have been reported. [from GeneReviews]

MedGen UID:
338072
Concept ID:
C1850554
Disease or Syndrome
2.

Restrictive ventricular septal defect

Any ventricular septal defect (VSD) that is small enough to restrict flow across it such that a pressure gradient exists between the two sides of the VSD. [from HPO]

MedGen UID:
488872
Concept ID:
C0344924
Congenital Abnormality

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