| Disease Browser
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Parent Node:
 Epidermodysplasia Verruciformis (D004819) |
Parent Node:
Genetic Diseases, X-Linked (D040181) |
..Starting node
.. Epidermodysplasia Verruciformis, X-Linked (C564430)
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Child Nodes:
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Sister Nodes: |
..Aarskog Syndrome (C535331)  1
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..Abruzzo Erickson syndrome (C535559)
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..Achromatopsia incomplete, X-linked (C538165)
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..Adrenal Hypoplasia, Congenital, with Precocious Puberty (C564568)
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..Agammaglobulinemia, X-linked, type 2 (C538057)
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..Aicardi Syndrome (D058540) 1
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..Aland Island Eye Disease (C562664)
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..Alpha-Thalassemia Myelodysplasia Syndrome (C563023)
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..Alport Syndrome, Mental Retardation, Midface Hypoplasia, and Elliptocytosis (C564570)
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..Alzheimer Disease 16 (C567463)
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..Androgen-Insensitivity Syndrome (D013734) 2
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..Anemia, Nonspherocytic Hemolytic, Due To G6pd Deficiency (C567533)
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..Anemia, sideroblastic spinocerebellar ataxia (C536358)
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..Anemia, X-Linked, without Thrombocytopenia (C564429)
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..Anencephaly and spina bifida X-linked (C536359)
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..Aneurysm, Intracranial Berry, 5 (C563670)
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..Angioma serpiginosum, X-linked (C536366)
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..Arthrogryposis multiplex congenita, distal, X-linked (C535380)
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..Arthrogryposis, X-Linked, Type V (C564574)
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..Arts syndrome (C535388)
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..Atypical Mycobacteriosis, Familial, X-Linked 1 (C567070)
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..Atypical Mycobacteriosis, Familial, X-Linked 2 (C567068)
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..Barth Syndrome (D056889) 2
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..Bornholm Eye Disease (C564092)
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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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..Branchial arch syndrome X-linked (C537102)
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..Brunner Syndrome (C563156)
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..Bruton type agammaglobulinemia (C537409)
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..Bulbo-Spinal Atrophy, X-Linked (D055534) 1
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..Bullous Dystrophy, Hereditary Macular Type (C563065)
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..Cantu syndrome (C535572)
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..Cardiac valvular dysplasia, X-linked (C535576)
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..Cardiomyopathy, Dilated, 3A (C564721)
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..Cataract, congenital, with microcornea or slight microphthalmia (C535338)
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..Chondrodysplasia punctata 2, X-linked dominant (C538416)
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..Chondrodysplasia punctata, brachytelephalangic (C535941)
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..Choroideremia (D015794) 2
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..Chromosome Xp11.23-P11.22 Duplication Syndrome (C567585)
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..Chromosome Xq28 Duplication Syndrome (C567580)
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..Cleft Palate with Ankyloglossia (C564442)
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..Cleft palate X-linked (C536426)
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..Cone Dystrophy, X-Linked, 1 (C564439)
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..Cone dystrophy, x-linked, with tapetal-like sheen (C535975)
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..Cone-Rod Dystrophy, X-Linked, 2 (C564717)
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..Cone-Rod Dystrophy, X-Linked, 3 (C564507)
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..Cone-Rod Dystrophy, X-Linked, Type 1 (C564438)
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..Congenital alopecia X-linked (C535981)
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..Congenital Heart Defects, X-Linked (C567444)
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..Congenital Hemidysplasia with Ichthyosiform Erythroderma and Limb Defects (C562515)
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..Congenital idiopathic intestinal pseudoobstruction (C535532)
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..Corpus Callosum, Partial Agenesis of, X-Linked (C564115)
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..Craniofacioskeletal Syndrome (C567471)
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..Deafness, High-Frequency Sensorineural, X-Linked (C564432)
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..Deafness, X-Linked 1 (C564433)
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..Deafness, X-Linked 3 (C564727)
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..Deafness, X-Linked 4 (C564723)
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..Deafness, X-Linked 5 (C564472)
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..Dent Disease (D057973) 1
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..Dent disease 1 (C538212)
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..Dent Disease 2 (C564487)
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..Dyggve-Melchior-Clausen syndrome (C535726)
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..Dyserythropoietic Anemia with Thrombocytopenia (C564525)
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..Dyskeratosis Congenita (D019871) 3
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..Dystonia 3, Torsion, X-Linked (C564048)
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..Ectodermal Dysplasia 1, Anhidrotic (D053358) 1
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..Ectodermal Dysplasia, Anhidrotic, with Immunodeficiency, Osteopetrosis, and Lymphedema (C564538)
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..Ectodermal dysplasia, hypohidrotic, with immune deficiency (C536181)
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..Ehlers-Danlos syndrome type 5 (C536197)
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..Epidermodysplasia Verruciformis, X-Linked (C564430)
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..Epilepsy, Female-Restricted, with Mental Retardation (C564715)
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..Epilepsy, X-Linked, with Variable Learning Disabilities and Behavior Disorders (C564505)
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..Episodic Muscle Weakness, X-Linked (C564565)
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..Exudative Vitreoretinopathy, Familial, X-Linked Recessive (C564428)
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..Fabry Disease (D000795) 2
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..Fetal akinesia syndrome, X-linked (C537921)
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..Fg Syndrome 5 (C564480)
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..Focal Dermal Hypoplasia (D005489) 1
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..Glycogen Storage Disease Type IIb (D052120)
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..Glycogen Storage Disease Type VIII (D006015)
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..Glycogen Storage Disease, Type IXA2 (C567579)
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..Glycogen Storage Disease, Type IXD (C564485)
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..Granulomatous Disease, Chronic (D006105) 7
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..Hemophilia B (D002836)
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..Heterotaxy, visceral, X-linked (C538116)
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..Heterotopia, Periventricular Nodular, with Frontometaphyseal Dysplasia (C564725)
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..Heterotopia, Periventricular, Ehlers-Danlos Variant (C564492)
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..Hodgkin disease, X-linked pseudoautosomal (C538326)
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..Hydrocephalus With Cerebellar Agenesis (C564407)
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..Hydrocephalus, X-linked (C536078)
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..Hydrocephalus, X-Linked, with Congenital Idiopathic Intestinal Pseudoobstruction (C564408)
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..Hyper-IgM Immunodeficiency Syndrome, Type 1 (D053307) 1
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..Hyperekplexia and Epilepsy (C564474)
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..Hypertrichosis congenital generalized X-linked (C538388)
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..Hypogammaglobulinemia and Isolated growth hormone deficiency, X-linked (C537149)
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..Hypogammaglobulinemia, X-Linked (C562478)
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..Hypoparathyroidism, X-Linked (C562782)
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..Hypospadias 1, X-Linked (C567482)
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..Hypospadias 2, X-Linked (C567462)
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..Ichthyosis, X-Linked (D016114) 2
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..Ichthyosis, X-Linked, Complicated (C567443)
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..Immune Dysregulation, Polyendocrinopathy, Enteropathy, X-Linked Syndrome (C580192)
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..Immunodeficiency, X-Linked, with Deficiency of 115,000 Dalton Surface Glycoprotein (C564120)
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..Immunodysregulation, Polyendocrinopathy, and Enteropathy, X-Linked (C562780)
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..Isolated Noncompaction of the Ventricular Myocardium (D056830) 5
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..Joubert Syndrome 10 (C567582)
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..Keratosis Follicularis Spinulosa Decalvans, X-Linked (C536159)
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..Leigh Syndrome, X-Linked (C564114)
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..Leukoencephalopathy With Metaphyseal Chondrodysplasia (C567065)
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..Liver Glycogenosis, X-Linked, Type II (C564421)
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..Lymphoproliferative Syndrome, X-Linked, 2 (C564469)
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..Macrothrombocytopenia, X-Linked (C564526)
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..Macular Dystrophy, X-Linked (C564110)
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..Major Affective Disorder 2 (C564108)
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..Martin-Probst Deafness-Mental Retardation Syndrome (C564495)
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..MASA (Mental Retardation, Aphasia, Shuffling Gait, Adducted Thumbs) Syndrome (C536029)
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..Megalocornea (C562829)
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..Membranoproliferative Glomerulonephritis, X-Linked (C564423)
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..Mental Retardation, Skeletal Dysplasia, and Abducens Palsy (C564101)
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..Mental Retardation, X-Linked (D038901) 134
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..Mental Retardation, X-Linked, Syndromic 12 (C564106)
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..Mental Retardation, X-Linked, Syndromic, Christianson Type (C567484)
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..Mental Retardation, X-Linked, Syndromic, Turner Type (C567476)
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..Mental Retardation, X-Linked, Syndromic, Zdhhc9-Related (C567586)
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..Mental Retardation, X-Linked, With Panhypopituitarism (C567485)
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..Mental Retardation, X-Linked, Znf711-Related (C567583)
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..Microcephaly microcornea syndrome Seemanova type (C537539)
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..Microphthalmia, Isolated, with Coloboma 1 (C564531)
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..Microphthalmia, syndromic 7 (C537466)
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..Midline Defects, X-Linked (C564054)
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..Mitral valve prolapse, familial, X-linked (C537478)
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..Modifier, X-Linked, for Neurofunctional Defects (C564098)
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..Multiple Pterygium Syndrome, X-Linked (C564072)
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..Muscular Dystrophy, Duchenne (D020388) 1
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..Muscular Dystrophy, Emery-Dreifuss (D020389) 10
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..Muscular Dystrophy, Progressive Pectorodorsal (C564095)
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..Myopathy, Reducing Body, X-Linked, Childhood-Onset (C567468)
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..Myopathy, Reducing Body, X-Linked, Early-Onset, Severe (C567469)
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..Myopathy, X-Linked, with Excessive Autophagy (C564093)
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..Myopia 1 (C564091)
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..Myopia 13 (C564473)
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..Nance-Horan syndrome (C538336)
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..Nasodigitoacoustic syndrome (C538337)
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..NEMO mutation with immunodeficiency (C538399)
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..Nephrogenic Syndrome of Inappropriate Antidiuresis (C564491)
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..Nephrolithiasis, X-Linked Recessive, with Renal Failure (C562901)
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..Neural tube defects X-linked (C536410)
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..Neuropathy, Hereditary Sensory, X-Linked (C564090)
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..Neutropenia, Severe Congenital, X-Linked (C564539)
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..Night blindness, congenital stationary (C536122) 4
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..Nystagmus 5, Infantile Periodic Alternating (C564478)
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..Oculocerebrorenal Syndrome (D009800) 1
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..Ophthalmoplegia, External, and Myopia (C564087)
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..Opitz GBBB Syndrome, X-Linked (C567932)
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..Optic atrophy, X-linked (C537125)
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..Ornithine Carbamoyltransferase Deficiency Disease (D020163) 1
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..Ovarian Dysgenesis 2 (C564499)
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..Panhypopituitarism X-linked (C538613)
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..Parathyroid Glands, Agenesis Of (C563238)
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..Parkinson Disease 12 (C564486)
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..Parkinsonism, early onset with mental retardation (C537179)
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..Pelizaeus-Merzbacher Disease (D020371) 1
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..Phosphoglycerate Kinase 1 Deficiency (C567067)
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..Pigmentary Disorder, Reticulate, with Systemic Manifestations (C564461)
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..Premature Ovarian Failure 2a (C564498)
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..Progressive hearing loss stapes fixation (C536424)
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..Properdin Deficiency, Type II (C564075)
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..Properdin Deficiency, Type III (C564076)
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..Properdin deficiency, X-linked (C537241)
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..PROSTATE CANCER, HEREDITARY, X-LINKED 1 (OMIM:300147)
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..Prostate Cancer, Hereditary, X-Linked 2 (C567477)
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..Protoporphyria, Erythropoietic, X-Linked Dominant (C567464)
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..Proud Syndrome (C563110)
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..Ptosis, Hereditary Congenital 2 (C564553)
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..Radial Ray Deficiency, X-Linked (C564523)
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..Radiation Sensitivity of Natural Killer Activity (C564066)
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..Radius absent anogenital anomalies (C535281)
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..Reticuloendotheliosis, X-linked (C538362)
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..Retinitis Pigmentosa 3 (C564520)
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..Retinitis Pigmentosa 34 (C564475)
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..Retinitis Pigmentosa 6 (C564065)
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..Retinitis Pigmentosa, X-Linked, And Sinorespiratory Infections, With Or Without Deafness (C567595)
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..Rolandic Epilepsy, Mental Retardation, and Speech Dyspraxia, X-Linked (C564467)
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..Russell-Silver Syndrome, X-Linked (C562446)
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..Short Stature, Idiopathic, X-Linked (C564479)
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..Simpson-Golabi-Behmel syndrome (C537340)
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..Simpson-Golabi-Behmel Syndrome, Type 2 (C564567)
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..Sketetal dysplasia coarse facies mental retardation (C536671)
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..Spastic paraplegia 16, X-linked (C536643)
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..Spastic paraplegia 2, X-linked (C536857)
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..Spastic Paraplegia 34, X-Linked (C567465)
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..Spina Bifida, X-Linked (C564459)
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..Spinal Muscular Atrophy, Distal, X-Linked 3 (C564506)
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..Spinocerebellar Ataxia, X-Linked 1 (C563134)
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..Spinocerebellar Ataxia, X-Linked 5 (C567478)
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..Spinocerebellar ataxia, X-linked, 3 (C537315)
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..Split-Hand Foot Malformation 2 (C564056) 1
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..Spondyloepimetaphyseal Dysplasia, X-Linked (C564714)
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..Spondyloepiphyseal Dysplasia Tarda, X-Linked (C562447)
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..Spondylometaphyseal Dysplasia, X-Linked (C563124)
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..Surfactant Metabolism Dysfunction, Pulmonary, 4 (C567461)
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..TERMINAL OSSEOUS DYSPLASIA (OMIM:300244)
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..Terminal Osseous Dysplasia and Pigmentary Defects (C564554)
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..Testicular Germ Cell Tumor 1 (C564559)
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..Thrombocytopenia 1 (C564052)
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..Thrombocytopenia, Platelet Dysfunction, Hemolysis, and Imbalanced Globin Synthesis (C564050)
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..Thrombocytopenia, X-Linked, Intermittent (C564053)
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..Thrombocytosis, Familial X-Linked (C564532)
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..Thrombophilia, X-Linked, Due To Factor Ix Defect (C567581)
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..Thyroxine-Binding Globulin Deficiency (C564049)
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..Tooth Agenesis, Selective, X-Linked, 1 (C567060)
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..Torticollis keloids cryptorchidism renal dysplasia (C536970)
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..VACTERL Association With Hydrocephalus (C564751)
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..VACTERL association with hydrocephaly, X-linked (C536520)
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..Vasquez Hurst Sotos syndrome (C536533)
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..Vesicoureteral Reflux, X-Linked (C564042)
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..Von Willebrand Disease, X-Linked Form (C564041)
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..Wells Jankovic syndrome (C536692)
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..Wieacker syndrome (C536703)
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..Wiskott-Aldrich Syndrome (D014923) 1
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..X Inactivation, Familial Skewed, 1 (C564716)
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..X Inactivation, Familial Skewed, 2 (C564572)
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..X-linked adrenal hypoplasia congenita (C536757)
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..X-Linked Chondrodysplasia Punctata 1 (C580533)
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..X-Linked Combined Immunodeficiency Diseases (D053632) 1
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..X-Linked Infantile Nystagmus (C580539)
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..X-linked sideroblastic anemia (C536761)
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..X-linked tetra-amelia (C536497)
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Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
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