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  Domain Name: FH
FORKHEAD. FORKHEAD, also known as a "winged helix"
No pairwise interactions found for the domain FH

Total Mutations Found: 41
Total Disease Mutations Found: 35
This domain occurred 51 times on human genes (93 proteins).



  ALVEOLAR CAPILLARY DYSPLASIA WITH MISALIGNMENT OF PULMONARY VEINS
  AXENFELD ANOMALY
  AXENFELD ANOMALY, INCLUDED;;
  AXENFELD-RIEGER ANOMALY
  AXENFELD-RIEGER SYNDROME, TYPE 3
  AXENFELD-RIEGER SYNDROME, TYPE 3, INCLUDED;;
  BLEPHAROPHIMOSIS, PTOSIS, AND EPICANTHUS INVERSUS, TYPE I
  DEVELOPMENTAL VERBAL DYSPRAXIA
  HYPOTHYROIDISM, ATHYROIDAL, WITH SPIKY HAIR AND CLEFT PALATE
  HYPOTHYROIDISM, THYROIDAL, WITH SPIKY HAIR AND CLEFT PALATE
  IMMUNODYSREGULATION, POLYENDOCRINOPATHY, AND ENTEROPATHY, X-LINKED
  LYMPHEDEMA-DISTICHIASIS SYNDROME
  MENTAL RETARDATION WITH LANGUAGE IMPAIRMENT AND AUTISTIC FEATURES
  PETERS ANOMALY, INCLUDED
  RETT SYNDROME, CONGENITAL VARIANT
  RIEGER ANOMALY


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Range on the Protein:  

   Protein ID            Protein Position

Domain Position:  


No Conserved Features/Sites Found for FH








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Please Cite: Peterson, T.A., Adadey, A., Santana-Cruz ,I., Sun, Y., Winder A, Kann, M.G., (2010) DMDM: Domain Mapping of Disease Mutations. Bioinformatics 26 (19), 2458-2459.

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