Hidrotic Ectodermal Dysplasia, Christianson-Fourie Type
hypohidrotic ectodermal dysplasia +
Johanson-Blizzard syndrome
Jones Hersh Yusk Syndrome
junctional epidermolysis bullosa with pyloric atresia
Ladda Zonana Ramer Syndrome
Lelis Syndrome
linear skin defects with multiple congenital anomalies 2
Marshall syndrome +
Naegeli-Franceschetti-Jadassohn syndrome
NEMO Mutation with Immunodeficiency
Neurocutaneous Syndromes +
nonsyndromic aplasia cutis congenita
A skin disease characterized by localized areas of missing skin that resemble ulcers or oopen wounds in new borns and that has_material_basis_in heterozygous mutation in the BMS1 gene on chromosome 10q11. (DO)
oculoectodermal syndrome
Odontomicronychial Dysplasia
Odontoonychodermal Dysplasia
Odontotrichoungual-Digital-Palmar Syndrome
Ohdo syndrome +
orofacial cleft 7 +
pachyonychia congenita +
palmoplantar keratoderma and congenital alopecia 1
palmoplantar keratoderma and congenital alopecia 2
Papillon-Lefevre disease +
photosensitive trichothiodystrophy 1
Pinheiro Freire-Maia Miranda Syndrome
pure hair and nail ectodermal dysplasia +
Rapp-Hodgkin syndrome
Robinson Miller Bensimon Syndrome
Rosselli-Gulienetti Syndrome
scalp-ear-nipple syndrome
Schinzel Giedion syndrome
Schopf-Schulz-Passarge syndrome
Sener Syndrome
Seres-Santamaria Arimany Muniz Syndrome
Taurodontia, Absent Teeth, Sparse Hair
Tetra Amelia with Ectodermal Dysplasia and Lacrimal Duct Abnormalities