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Items: 2

1.

Brachydactyly, type A2, with microcephaly

MedGen UID:
395250
Concept ID:
C1859393
Disease or Syndrome
2.

Type A2 brachydactyly

Brachydactyly type A2 is an autosomal dominant disorder characterized by malformations of the middle phalanx of the index finger and by anomalies of the second toe (summary by Su et al., 2011). [from OMIM]

MedGen UID:
318690
Concept ID:
C1832702
Congenital Abnormality

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