- A -
AREDYLD Syndrome [MESH:C537427] (1)
Adams Oliver syndrome [MESH:C538225] (1)
Alves Castelo dos Santos syndrome [MESH:C536593] (1)
Anal sphincter dysplasia [MESH:C538254] (1)
Aplasia Cutis Congenita with Epibulbar Dermoids [MESH:C563969] (1)
Aplasia Cutis Congenita, Congenital Heart Defect, And Frontonasal Cysts [MESH:C566997] (1)
Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction [MESH:C563394] (1)
Aplasia cutis congenita intestinal lymphangiectasia [MESH:C537788] (1)
Aplasia cutis congenita of limbs recessive [MESH:C536840] (1)
Arthrogryposis and ectodermal dysplasia [MESH:C537441] (1)
- B -
Basan syndrome [MESH:C537659] (1)
Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear/Eye Anomalies, Cleft Palate/Cryptorchidism, And Kidney Dysplasia/Hypoplasia [MESH:C564519] (1)
Brunoni syndrome [MESH:C537408] (1)
- C -
Cardiofaciocutaneous syndrome [MESH:C535579] (407)
Cerebellar ataxia ectodermal dysplasia [MESH:C535350] (1)
Cleft Lip with or without Cleft Palate, Nonsyndromic, 8 [MESH:C565070] (1)
Congenital ectodermal dysplasia with hearing loss [MESH:C535757] (1)
Contractures ectodermal dysplasia cleft lip palate [MESH:C535465] (1)
Cranioectodermal Dysplasia [MESH:C562966] (16)
- D -
Deafness with Anhidrotic Ectodermal Dysplasia [MESH:C565119] (1)
Dermatoosteolysis Kirghizian type [MESH:C535373] (1)
- E -
Ectodermal Dysplasia 1, Anhidrotic [MESH:D053358] (11)
Ectodermal Dysplasia 3, Anhidrotic [MESH:D053359] (10)
Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet [MESH:C565067] (1)
Ectodermal Dysplasia and Neurosensory Deafness [MESH:C565606] (1)
Ectodermal Dysplasia with Natal Teeth, Turnpenny Type [MESH:C563347] (1)
Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant [MESH:C567411] (533)
Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema [MESH:C564538] (56)
Ectodermal Dysplasia, Hidrotic, Autosomal Recessive [MESH:C566553] (1)
Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive [MESH:D053360] (10)
Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Agenesis of the Corpus Callosum [MESH:C565605] (1)
Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Ciliary Dyskinesia [MESH:C565604] (1)
Ectodermal Dysplasia, Pure Hair-Nail Type [MESH:C566592] (1)
Ectodermal Dysplasia, Trichoodontoonychial Type [MESH:C565068] (1)
Ectodermal dysplasia adrenal cyst [MESH:C538015] (1)
Ectodermal dysplasia alopecia preaxial polydactyly [MESH:C538016] (1)
Ectodermal dysplasia mental retardation syndactyly [MESH:C538018] (1)
Ectodermal dysplasia, ectrodactyly, and macular dystrophy [MESH:C536190] (34)
Ectodermal dysplasia, hidrotic, Christianson-Fourie type [MESH:C536180] (1)
Ectodermal dysplasia, hypohidrotic, with immune deficiency [MESH:C536181] (56)
Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features [MESH:C536182] (1)
Ectodermal dysplasia/ skin fragility syndrome [MESH:C536183] (20)
Ectrodactyly and Ectodermal Dysplasia without Cleft Lip/Palate [MESH:C565065] (1)
Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip/Palate Syndrome 1 [MESH:C565062] (1)
Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip/Palate Syndrome 3 [MESH:C565799] (46)
Ectrodactyly-cleft lip/palate syndrome [MESH:C536189] (46)
Ellis-Van Creveld Syndrome [MESH:D004613] (50)
Epidermolysis bullosa with pyloric atresia [MESH:C535377] (1)
Euhidrotic ectodermal dysplasia [MESH:C535763] (1)
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- F -
Focal Dermal Hypoplasia [MESH:D005489] (22)
Focal facial dermal dysplasia [MESH:C537068] (1)
Freire-Maia odontotrichomelic syndrome [MESH:C535637] (1)
- H -
Halal Setton Wang syndrome [MESH:C535621] (1)
Hay Wells syndrome recessive type [MESH:C535846] (1)
Hay-Wells syndrome [MESH:C535847] (46)
Hyper-IgM Immunodeficiency, X-Linked, with Ectodermal Dysplasia, Hypohidrotic [MESH:C564542] (1)
- J -
Johanson Blizzard syndrome [MESH:C535880] (17)
Jones Hersh Yusk syndrome [MESH:C535885] (1)
- L -
Ladda Zonana Ramer syndrome [MESH:C538135] (1)
Lelis Syndrome [MESH:C564261] (1)
- M -
Madokoro Ohdo Sonoda syndrome [MESH:C537838] (1)
- N -
NEMO mutation with immunodeficiency [MESH:C538399] (1)
Naegeli syndrome [MESH:C538331] (38)
Neurocutaneous Syndromes [MESH:D020752] (39)
- O -
Odontomicronychial dysplasia [MESH:C537741] (1)
Odontoonychodermal dysplasia [MESH:C537742] (21)
Odontotrichoungual-Digital-Palmar Syndrome [MESH:C566598] (1)
Orofacial Cleft 7 [MESH:C563464] (1)
- P -
Pachyonychia Congenita [MESH:D053549] (80)
Pinheiro Freire-Maia Miranda syndrome [MESH:C537402] (1)
Propping Zerres syndrome [MESH:C538052] (46)
- R -
Rapp-Hodgkin syndrome [MESH:C535289] (46)
Robinson Miller Bensimon syndrome [MESH:C535864] (1)
Rosselli-Gulienetti Syndrome [MESH:C563117] (25)
- S -
Sener syndrome [MESH:C537579] (1)
Seres-Santamaria Arimany Muniz syndrome [MESH:C537585] (1)
- T -
Taurodontia absent teeth sparse hair [MESH:C536945] (1)
Tetra amelia with ectodermal dysplasia and lacrimal duct abnormalities [MESH:C536496] (1)
Trichodental syndrome [MESH:C536551] (1)
Trichoodontoonychial Dysplasia [MESH:C564760] (1)
Trichoscyphodysplasia [MESH:C536557] (1)
Trueb Burg Bottani syndrome [MESH:C536565] (1)
- Y -
Yunis Varon syndrome [MESH:C536719] (1)
- Z -
Zlotogora-Ogur syndrome [MESH:C536726] (25)
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