OMIM

• OMIM Links for Nucleotide (Select 15149011) (1)
  OMIM
• Homo sapiens cDNA clone IMAGE:5285105, containing frame-shift errors
  Homo sapiens cDNA clone IMAGE:5285105, containing frame-shift errors

  gi|23271284|gb|BC036069.1|
  Nucleotide
• Netherton Syndrome
  Netherton Syndrome

  Rare autosomal recessive disease with variable expressions. Clinical features of the disease include variable ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL; bamboo hair (trichorrhexi...<br/>Year introduced: 2010
  MeSH
• Ichthyosiform Erythroderma, Congenital
  Ichthyosiform Erythroderma, Congenital

  Designation for several severe forms of ichthyosis, present at birth, that are characterized by hyperkeratotic scaling. Infants may be born encased in a collodion membrane whi...<br/>Year introduced: 1991
  MeSH
• Focal Facial Dermal Dysplasias
  Focal Facial Dermal Dysplasias

  A heterogenous group of genetic disorders characterized by scar-like atrophic lesions on the temple region of the head including preauricular area. Location of skin defects is...<br/>Year introduced: 2022
  MeSH

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