| Disease Browser
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Parent Node:
 Cerebellar Ataxia (D002524) |
Parent Node:
Ectodermal Dysplasia (D004476) |
..Starting node
.. Cerebellar ataxia ectodermal dysplasia (C535350)
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Child Nodes:
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Sister Nodes: |
..Adams Oliver syndrome (C538225)
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..Alves Castelo dos Santos syndrome (C536593)
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..Anal sphincter dysplasia (C538254)
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..Aplasia cutis congenita intestinal lymphangiectasia (C537788)
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..Aplasia cutis congenita of limbs recessive (C536840)
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..Aplasia Cutis Congenita with Epibulbar Dermoids (C563969)
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..Aplasia Cutis Congenita, Congenital Heart Defect, And Frontonasal Cysts (C566997)
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..Aplasia Cutis Congenita, High Myopia, and Cone-Rod Dysfunction (C563394)
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..AREDYLD Syndrome (C537427)
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..Arthrogryposis and ectodermal dysplasia (C537441)
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..Basan syndrome (C537659)
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..Brain Anomalies, Retardation, Ectodermal Dysplasia, Skeletal Malformations, Hirschsprung Disease, Ear-Eye Anomalies, Cleft Palate-Cryptorchidism, And (C564519)
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..Brunoni syndrome (C537408)
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..Cardiofaciocutaneous syndrome (C535579)
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..Cerebellar ataxia ectodermal dysplasia (C535350)
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..Cleft Lip with or without Cleft Palate, Nonsyndromic, 8 (C565070)
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..Congenital ectodermal dysplasia with hearing loss (C535757)
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..CONGENITAL HEART DEFECTS AND ECTODERMAL DYSPLASIA (OMIM:617364)
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..Contractures ectodermal dysplasia cleft lip palate (C535465)
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..Cranioectodermal Dysplasia (C562966)  1
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..Deafness with Anhidrotic Ectodermal Dysplasia (C565119)
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..Dermatoosteolysis Kirghizian type (C535373)
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..Ectodermal Dysplasia 1, Anhidrotic (D053358) 1
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..ECTODERMAL DYSPLASIA 11A, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL DOMINANT (OMIM:614940)
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..ECTODERMAL DYSPLASIA 12, HYPOHIDROTIC/HAIR/TOOTH/NAIL TYPE (OMIM:617337)
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..ECTODERMAL DYSPLASIA 13, HAIR/TOOTH TYPE (OMIM:617392)
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..Ectodermal Dysplasia 3, Anhidrotic (D053359)
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..ECTODERMAL DYSPLASIA 4, HAIR/NAIL TYPE (OMIM:602032)
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..ECTODERMAL DYSPLASIA 7, HAIR/NAIL TYPE (OMIM:614929)
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..ECTODERMAL DYSPLASIA 9, HAIR/NAIL TYPE (OMIM:614931)
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..Ectodermal dysplasia adrenal cyst (C538015)
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..Ectodermal dysplasia alopecia preaxial polydactyly (C538016)
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..Ectodermal Dysplasia and Neurosensory Deafness (C565606)
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..Ectodermal dysplasia mental retardation syndactyly (C538018)
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..Ectodermal Dysplasia Syndrome with Distinctive Facial Appearance and Preaxial Polydactyly of Feet (C565067)
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..Ectodermal Dysplasia with Natal Teeth, Turnpenny Type (C563347)
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..Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema (C564538)
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..Ectodermal Dysplasia, Anhidrotic, With T-Cell Immunodeficiency, Autosomal Dominant (C567411)
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..Ectodermal dysplasia, ectrodactyly, and macular dystrophy (C536190)
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..Ectodermal Dysplasia, Hidrotic, Autosomal Recessive (C566553)
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..Ectodermal dysplasia, hidrotic, Christianson-Fourie type (C536180)
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..Ectodermal Dysplasia, Hypohidrotic, Autosomal Recessive (D053360)
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..Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Agenesis of the Corpus Callosum (C565605)
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..Ectodermal Dysplasia, Hypohidrotic, with Hypothyroidism and Ciliary Dyskinesia (C565604)
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..Ectodermal dysplasia, hypohidrotic, with immune deficiency (C536181)
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..Ectodermal Dysplasia, Pure Hair-Nail Type (C566592)
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..Ectodermal dysplasia, sensorineural hearing loss, and distinctive facial features (C536182)
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..Ectodermal Dysplasia, Trichoodontoonychial Type (C565068)
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..Ectodermal Dysplasia-Skin Fragility Syndrome (C536183)
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..ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 1 (OMIM:613573)
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..ECTODERMAL DYSPLASIA-SYNDACTYLY SYNDROME 2 (OMIM:613576)
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..ECTODERMAL DYSPLASIA/SHORT STATURE SYNDROME (OMIM:616029)
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..Ectrodactyly and Ectodermal Dysplasia without Cleft Lip-Palate (C565065)
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..Ectrodactyly, Ectodermal Dysplasia, And Cleft Lip-Palate Syndrome 1 (C565062)
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..Ectrodactyly, Ectodermal Dysplasia, and Cleft Lip-Palate Syndrome 3 (C565799)
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..Ectrodactyly-cleft lip-palate syndrome (C536189)
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..Ellis-Van Creveld Syndrome (D004613) 6
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..Epidermolysis bullosa with pyloric atresia (C535377)
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..Euhidrotic ectodermal dysplasia (C535763)
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..Facial ectodermal dysplasia (C536385)
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..Focal Dermal Hypoplasia (D005489) 1
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..Focal facial dermal dysplasia (C537068)
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..Freire-Maia odontotrichomelic syndrome (C535637)
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..Halal Setton Wang syndrome (C535621)
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..Hay Wells syndrome recessive type (C535846)
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..Hay-Wells syndrome (C535847)
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..Hyper-IgM Immunodeficiency, X-Linked, with Ectodermal Dysplasia, Hypohidrotic (C564542)
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..Johanson Blizzard syndrome (C535880)
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..Jones Hersh Yusk syndrome (C535885)
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..Ladda Zonana Ramer syndrome (C538135)
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..Lelis Syndrome (C564261)
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..LINEAR SKIN DEFECTS WITH MULTIPLE CONGENITAL ANOMALIES 2 (OMIM:300887)
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..Madokoro Ohdo Sonoda syndrome (C537838)
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..Naegeli syndrome (C538331)
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..NEMO mutation with immunodeficiency (C538399)
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..Neurocutaneous Syndromes (D020752) 42  C:1
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..Odontomicronychial dysplasia (C537741)
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..Odontoonychodermal dysplasia (C537742)
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..Odontotrichoungual-Digital-Palmar Syndrome (C566598)
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..Orofacial Cleft 7 (C563464)
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..Pachyonychia Congenita (D053549) 5
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..Pinheiro Freire-Maia Miranda syndrome (C537402)
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..Propping Zerres syndrome (C538052)
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..Rapp-Hodgkin syndrome (C535289)
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..Robinson Miller Bensimon syndrome (C535864)
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..Rosselli-Gulienetti Syndrome (C563117)
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..Sener syndrome (C537579)
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..Seres-Santamaria Arimany Muniz syndrome (C537585)
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..Taurodontia absent teeth sparse hair (C536945)
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..Tetra amelia with ectodermal dysplasia and lacrimal duct abnormalities (C536496)
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..Trichodental syndrome (C536551)
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..Trichoodontoonychial Dysplasia (C564760)
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..Trichoscyphodysplasia (C536557)
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..TRICHOTHIODYSTROPHY 1, PHOTOSENSITIVE (OMIM:601675)
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..Trueb Burg Bottani syndrome (C536565)
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..Yunis Varon syndrome (C536719)
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..Zlotogora-Ogur syndrome (C536726)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM,ClinVar, CTD
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