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Results 1 - 10 of 17 for Aplasia cutis congenita
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  1. COL7A1 gene 
    ... of skin (also known as Bart syndrome or aplasia cutis congenita type VI). Individuals with this condition have patches of missing skin at birth (aplasia cutis congenita), typically on the legs. On other parts of ...
    https://medlineplus.gov/genetics/gene/col7a1 - Genetics
  2. EDA gene 
    ... EDA gene have been found to cause hypohidrotic ectodermal dysplasia, the most common form of ectodermal dysplasia. Starting before birth, ectodermal dysplasias result in the ...
    https://medlineplus.gov/genetics/gene/eda - Genetics
  3. ARHGAP31 gene 
    ... a condition characterized by areas of missing skin (aplasia cutis congenita), usually on the scalp, and malformations of the hands and feet. These mutations lead to production of an abnormally short ARHGAP31 protein that is more ... a Cdc42/Rac1 GTPase regulator, cause syndromic cutis aplasia and limb anomalies. Am J Hum Genet. 2011 ...
    https://medlineplus.gov/genetics/gene/arhgap31 - Genetics
  4. NOTCH1 gene 
    ... a condition characterized by areas of missing skin (aplasia cutis congenita), usually on the scalp, and malformations of the ...
    https://medlineplus.gov/genetics/gene/notch1 - Genetics
  5. RBPJ gene 
    ... a condition characterized by areas of missing skin (aplasia cutis congenita), usually on the scalp, and malformations of the ...
    https://medlineplus.gov/genetics/gene/rbpj - Genetics
  6. DLL4 gene 
    ... a condition characterized by areas of missing skin (aplasia cutis congenita), usually on the scalp, and malformations of the ...
    https://medlineplus.gov/genetics/gene/dll4 - Genetics
  7. DOCK6 gene 
    ... a condition characterized by areas of missing skin (aplasia cutis congenita), usually on the scalp, and malformations of the ...
    https://medlineplus.gov/genetics/gene/dock6 - Genetics
  8. EOGT gene 
    ... condition is characterized by areas of missing skin (aplasia cutis congenita), usually on the scalp, and malformations of the ...
    https://medlineplus.gov/genetics/gene/eogt - Genetics
  9. EDARADD gene 
    ... EDARADD gene have been found to cause hypohidrotic ectodermal dysplasia, the most common form of ectodermal dysplasia. Starting before birth, ectodermal dysplasias result in the ...
    https://medlineplus.gov/genetics/gene/edaradd - Genetics
  10. EDAR gene 
    ... EDAR gene have been found to cause hypohidrotic ectodermal dysplasia, the most common form of ectodermal dysplasia. Starting before birth, ectodermal dysplasias result in the ...
    https://medlineplus.gov/genetics/gene/edar - Genetics
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