craniometaphyseal dysplasia (Q3710209)

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osteosclerosis that has material basis in mutations in the ANKH gene which results in progressive thickening located in skull and abnormally shaped ends of long bones in the limbs
  • Craniometaphyseal dysplasia
  • CMDD
  • CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CMDD
  • CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT
  • Cmd
  • Craniometaphyseal Dysplasia, Jackson Type
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Language Label Description Also known as
English
craniometaphyseal dysplasia
osteosclerosis that has material basis in mutations in the ANKH gene which results in progressive thickening located in skull and abnormally shaped ends of long bones in the limbs
  • Craniometaphyseal dysplasia
  • CMDD
  • CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT; CMDD
  • CRANIOMETAPHYSEAL DYSPLASIA, AUTOSOMAL DOMINANT
  • Cmd
  • Craniometaphyseal Dysplasia, Jackson Type

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