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Items: 4

1.

Brachydactyly type B1

A rare subtype of brachydactyly type B characterized by hypoplasia or aplasia of the distal phalanges of digits 2-5 with or without nail dysplasia, in association with fusion of the middle and distal phalanges, a broad or bifid thumb, and occasionally distal and proximal symphalangism or syndactyly. The feet are less severely affected than the hands. [from ORDO]

MedGen UID:
349432
Concept ID:
C1862112
Congenital Abnormality; Finding
2.

Yunis-Varon syndrome

Yunis-Varon syndrome (YVS) is a severe autosomal recessive disorder characterized by skeletal defects, including cleidocranial dysplasia and digital anomalies, and severe neurologic involvement with neuronal loss. Enlarged cytoplasmic vacuoles are found in neurons, muscle, and cartilage. The disorder is usually lethal in infancy (summary by Campeau et al., 2013). [from OMIM]

MedGen UID:
341818
Concept ID:
C1857663
Disease or Syndrome
3.

Brachydactyly type B2

Brachydactyly type B2 (BDB2) is a subtype of brachydactyly characterized by hypoplasia/aplasia of distal phalanges in combination with distal symphalangism, fusion of carpal/tarsal bones, and partial cutaneous syndactyly (summary by Lehmann et al., 2007). [from OMIM]

MedGen UID:
409880
Concept ID:
C1969652
Disease or Syndrome
4.

Aplasia/Hypoplasia of the distal phalanges of the hand

Absence or underdevelopment of the distal phalanges. [from HPO]

MedGen UID:
396110
Concept ID:
C1861336
Finding
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