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Items: 3

1.

Oculodentodigital dysplasia, autosomal recessive

Autosomal recessive form of oculodentodigital dysplasia. [from MONDO]

MedGen UID:
412708
Concept ID:
C2749477
Disease or Syndrome
2.

Tall stature-scoliosis-macrodactyly of the great toes syndrome

Miura-type epiphyseal chondrodysplasia (ECDM) is an overgrowth syndrome characterized by tall stature, arachnodactyly of the hands, macrodactyly of the great toes, scoliosis, coxa valga, and slipped capital femoral epiphysis (Miura et al., 2014). Multiple extra epiphyses are present in the hands (Boudin et al., 2018). Mutation in the NPR3 gene (108962) results in Boudin-Mortier syndrome (BOMOS; 619543), a similar phenotype of tall stature, arachnodactyly, elongated great toes, and multiple extra epiphyses. [from OMIM]

MedGen UID:
863127
Concept ID:
C4014690
Disease or Syndrome
3.

Fifth finger distal phalanx clinodactyly

Bending or curvature of the distal phalanx of little finger in the radial direction (i.e., towards the 4th finger). [from HPO]

MedGen UID:
870685
Concept ID:
C4025139
Congenital Abnormality
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