Ontomatica – ChEMATIC (Wedge)

The current query selects 958 items in 84 groups, which could be too many to show at once. If you are sure you want to see them all, you can proceed to see the entire category, 'or select a more specific subcategory of "Ectodermal Dysplasia [MESH:D004476]" below.

Subcategories in Congenital, Hereditary, and Neonatal Diseases and Abnormalities [MESH:D009358] > Congenital Abnormalities [MESH:D000013] > Skin Abnormalities [MESH:D012868] > Ectodermal Dysplasia [MESH:D004476]:
(jump to A - B - C - D - E - F - H - J - L - M - N - O - P - R - S - T - Y - Z)

- 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)

- 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)