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Results 1 - 8 of 8 for Ectodermal dysplasia "5," "hair/nail" type
  1. Hypohidrotic ectodermal dysplasia 
    ... Touraine syndrome CST syndrome HED Genetic Testing Registry: Ectodermal dysplasia 10A, hypohidrotic/hair/nail type, autosomal dominant Genetic Testing Registry: Ectodermal dysplasia 10B, ...
    https://medlineplus.gov/.../hypohidrotic-ectodermal-dysplasia - Genetics
  2. WNT10A gene 
    ... protein disrupts Wnt signaling during the development of ectodermal tissues, including the skin, hair, nails, teeth, and sweat ... SYNDROME; SSPS ODONTOONYCHODERMAL DYSPLASIA; OODD WINGLESS-TYPE MMTV INTEGRATION SITE FAMILY, MEMBER ...
    https://medlineplus.gov/genetics/gene/wnt10a - Genetics
  3. Clouston syndrome 
    ... Clouston hidrotic ectodermal dysplasia Clouston's syndrome ECTD2 Ectodermal dysplasia 2, Clouston type HED2 Hidrotic ectodermal dysplasia 2 Genetic Testing Registry: ...
    https://medlineplus.gov/genetics/condition/clouston-syndrome - Genetics
  4. WDR35 gene 
    ... WDR35 gene mutations can cause short-rib polydactyly type 5, a severe condition with signs and symptoms similar ... to birth. Bone abnormalities in short-rib polydactyly type 5 include extremely short ribs, short arms and legs, ...
    https://medlineplus.gov/genetics/gene/wdr35 - Genetics
  5. WDR19 gene 
    ... bones; and abnormalities of certain tissues known as ectodermal tissues, which include the teeth, hair, nails, and skin. Cranioectodermal dysplasia can also cause a variety of other problems, ...
    https://medlineplus.gov/genetics/gene/wdr19 - Genetics
  6. IFT43 gene 
    ... bones; and abnormalities of certain tissues known as ectodermal tissues, which include the teeth, hair, nails, and skin.The IFT43 gene mutation involved in cranioectodermal dysplasia leads to production of an abnormally short IFT43 ...
    https://medlineplus.gov/genetics/gene/ift43 - Genetics
  7. IFT122 gene 
    ... bones; and abnormalities of certain tissues known as ectodermal tissues, which include the teeth, hair, nails, and skin.At least six IFT122 gene mutations have been found in people with cranioectodermal dysplasia. These mutations reduce the amount or function of ...
    https://medlineplus.gov/genetics/gene/ift122 - Genetics
  8. KRT14 gene 
    ... This disorder is a rare form of ectodermal dysplasia, a group of about 150 conditions characterized by abnormal development of ectodermal tissues including the skin, hair, nails, teeth, and sweat glands. NFJS and DPR were ...
    https://medlineplus.gov/genetics/gene/krt14 - Genetics