Preface

Jarind's Letters

Sims'Letters

Genetic Lists

Prevention

Letters of Signs

Genetic Lists of Abnormal Genes ( Lists of Sims' Letters)

 

S = Skin,hair & nail system

    
Neurofibromatosis   Anhidrotic
                                     ectodermal dysplasia

s1 = Albinism type I(Oculocutaneous)
autosomal recessive
s2 = Albinism type II(Oculocutaneous albinoidism)
autosomal recessive
s3 = Albinism type III(Chediak-Higashi syndrome)
autosomal recessive
s4 = Albinism type IV autosomal recessive
(Oculocutaneous albinism with congenital deafness)
s5 = Atopic Dermatitis multifactorial inheritance
S6 = Cafe-au-lait macules autosomal dominant
in Neurofibromatosis (Von Reckling hausen's disease)
s7 = Epidermolysis bullosa dystrophica(birth onset)
autosomal recessive (Scarring types)
S8 = Epidermolysis bullosa dystrophica(Infancy onset)
autosomal dominant (Scarring types)
S9 = Epidermolysis bullosa simplex(Birth onset)
autosomal dominant (Nonscarring type)
S10 = Epidermolysis dystrophica hereditaria
autosomal dominant
S11 = Epidermolytic hyperkeratosis
autosomal dominant
S12 =  Hairy body skin autosomal dominant
s13 = Hereditary anhidrotic ectodermal dysplasia
( X-linked recessive )
S14 = Hidrotic ectodermal dysplasia
autosomal dominant
s15 = Ichthyosis congenita
autosomal recessive
s16 = Ichthyosis simplex
( X-linked recessive )
S17 = Ichthyosis vulgaris
autosomal dominant
s18 = Junctional bullous epidermatosis (Herlitz Disease)
autosomal recessive (Nonscarring type)
s19 = Kinky hair syndrome(Menkes)
( X-linked recessive )
S20 = Pigmented macules on oral mucosa (Peutz-Jegher's syndrome)
autosomal dominant
S21 = Psoriasis vulgaris
( some incomplete penetrance )
autosomal dominant
S22 = Recurrent bullous eruption of hands & feet
(Weber-Cockayne syndrome) (Nonscarring type)
autosomal dominant
s23 = Skin defect ( in cleft lip )
multifactorial inheritance
s24 = Xeroderma pigmentosum
autosomal recessive
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Update since 10/09/50