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Table 2 Medical history

From: No evidence for preferential X-chromosome inactivation as the main cause of divergent phenotypes in sisters with X-linked hypohidrotic ectodermal dysplasia

Code Diseases other than XLHED Recurrent eye problems Hearing impairment
Photophobia Conjunctivitis
F1_S1 Allergy N N N
F1_S2 NAD N N N
F1_M NAD N N N
F2_S1 Urticaria, neurodermatitis Y Y Y
F2_S2 NAD Y N N
F2_M NAD Y N N
F3_S1 Diabetes Y N Y
F3_S2 NAD Y N N
F4_S1 NAD N N N
F4_S2 Hashimoto's thyroiditis N Y N
F4_M Hypothyroidism N Y N
F5_S1 Glaucoma Y N N
F5_S2 Hypothyroidism N N N
F6_S1 Hypothyroidism N N N
F6_S2 Allergy, eczema N N N
F6_M NAD N N N
  1. Abbreviations: F, family; S, sister; M, mother; NAD, no abnormality detected; Y, yes; N, no