Hearing Loss Disease Portal


 
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Most Common: Hearing Loss (D034381), Deafness (D003638), Sensorineural HL (D006319), Waardenburg Syndrome, Usher Syndromes
Disease Browser
Parent Node:
expandDermatitis (D003872)
Parent Node:
expandHypersensitivity, Immediate (D006969)
Parent Node:
expandSkin Diseases, Eczematous (D017443)
Parent Node:
expandSkin Diseases, Genetic (D012873)
..Starting node
..expandDermatitis, Atopic (D003876)

       Child Nodes:
........expandDeafness, Neural, with Atypical Atopic Dermatitis (C565639)
........expandDermatitis, Atopic, 1 (C566404)
........expandDermatitis, Atopic, 2 (C565293)
........expandDermatitis, Atopic, 3 (C565292)
........expandDermatitis, Atopic, 4 (C565291)
........expandDermatitis, Atopic, 5 (C565280)
........expandDermatitis, Atopic, 6 (C565279)
........expandDermatitis, Atopic, 7 (C567796)
........expandMOMES Syndrome (C564660)



 Sister Nodes: 
..expandActinic Prurigo (C566780)
..expandAlbinism (D000417) Child30
..expandAmyloidosis IX (C562643)
..expandAmyloidosis, Cutaneous Bullous (C562644)
..expandAmyloidosis, Primary Cutaneous (C562642)
..expandAnnular Erythema (C562461)
..expandArterial Tortuosity Syndrome (C565942)
..expandAtrophia Maculosa Varioliformis Cutis, Familial (C563349)
..expandBasaloid Follicular Hamartoma Syndrome, Generalized, Autosomal Dominant (C565284)
..expandBuschke-Ollendorff syndrome (C537415)
..expandCollagenosis, Familial Reactive Perforating (C565687)
..expandCutis Laxa (D003483) Child17
..expandDarier Disease (D007644) Child7
..expandDermatitis, Atopic (D003876) Child9
..expanddowling-degos disease (C562924)
..expandDyschromatosis universalis hereditaria (C535730)
..expandDyschromatosis Universalis Hereditaria 1 (C567273)
..expandDyschromatosis Universalis Hereditaria 2 (C567194)
..expandDyskeratosis Congenita (D019871) Child3
..expandEctodermal Dysplasia (D004476) Child144
..expandEhlers-Danlos Syndrome (D004535) Child23
..expandEpidermolysis Bullosa (D004820) Child29
..expandErythrokeratodermia Variabilis (D056266) Child3
..expandErythrokeratodermia with ataxia (C535738)
..expandExfoliative Ichthyosis, Autosomal Recessive, Ichthyosis Bullosa of Siemens-like (C564309)
..expandFingerprints, Absence of (C565010)
..expandFollicular Atrophoderma, Perioral Pigmented, with Milia and Epidermoid Cysts (C566360)
..expandGerodermia osteodysplastica (C537799)
..expandHereditary Autoinflammatory Diseases (D056660) Child10
..expandHistiocytic Dermatoarthritis (C564183)
..expandHyalinosis, Systemic (D057770)
..expandHyaluronan Metabolism, Defect in (C565742)
..expandIchthyosiform Erythroderma, Congenital (D016113) Child18
..expandIchthyosis Bullosa of Siemens (D053560)
..expandIchthyosis Vulgaris (D016112) Child1
..expandIchthyosis, X-Linked (D016114) Child2
..expandIncontinentia Pigmenti (D007184) Child2
..expandJuvenile Spring Eruption of Ears (C566781)
..expandKeratoderma, Palmoplantar (D007645) Child45
..expandKeratolytic winter erythema (C536155)
..expandKeratosis Follicularis Spinulosa Decalvans, X-Linked (C536159)
..expandKeratosis Linearis with Ichthyosis Congenita and Sclerosing Keratoderma (C566600)
..expandLeukokeratosis, Hereditary Mucosal (D053529)
..expandLeukomelanoderma, Infantilism, Mental Retardation, Hypodontia, Hypotrichosis (C565440)
..expandLipoid Proteinosis of Urbach and Wiethe (D008065)
..expandMonilethrix (D056734) Child1
..expandMuir-Torre Syndrome (D055653)
..expandNetherton Syndrome (D056770)
..expandNoduli Cutanei, Multiple, with Urinary Tract Abnormalities (C563512)
..expandOculotrichodysplasia (C564934)
..expandOnychogryposis, Pedal, with Keratosis Plantaris and Coarse Hair (C563506)
..expandOrofaciodigital syndrome 9 (C557818)
..expandOsseous Heteroplasia, Progressive (C562735)
..expandOsteopoikilosis, Isolated (C563484)
..expandParana Hard Skin Syndrome (C564905)
..expandPeeling Skin Syndrome (C564818)
..expandPemphigus, Benign Familial (D016506)
..expandPerifolliculitis Capitis Abscedens Et Suffodiens, Familial (C562486)
..expandPigmentary Disorder, Reticulate, with Systemic Manifestations (C564461)
..expandPlasminogen Deficiency, Type I (C566897)
..expandPoikiloderma, Hereditary Sclerosing (C562824)
..expandPorokeratosis (D017499) Child7
..expandPorphyria, Erythropoietic (D017092)
..expandPorphyrias, Hepatic (D017094) Child14
..expandProlidase Deficiency (D056732)
..expandPseudoxanthoma Elasticum (D011561) Child2
..expandRothmund-Thomson Syndrome (D011038) Child5
..expandSjogren-Larsson Syndrome (D016111) Child1
..expandSkin Fragility-Woolly Hair Syndrome (C564359)
..expandStiff Skin Syndrome (C566112)
..expandStorm Syndrome (C566109)
..expandTrichothiodystrophy Syndromes (D054463) Child5
..expandVitiligo, Progressive, with Mental Retardation and Urethral Duplication (C564739)
..expandVohwinkel Syndrome, Variant Form (C565826)
..expandXeroderma Pigmentosum (D014983) Child16
   

Human Disease MESH is developed by UMLS.
Further data from MedGen, OMIM, CTD
Term ID:3218
Name:Dermatitis, Atopic
Definition:A chronic inflammatory genetically determined disease of the skin marked by increased ability to form reagin (IgE), with increased susceptibility to allergic rhinitis and asthma, and hereditary disposition to a lowered threshold for pruritus. It is manifested by lichenification, excoriation, and crusting, mainly on the flexural surfaces of the elbow and knee. In infants it is known as infantile eczema.
Alternative IDs:
ParentIDs:MESH:D003872|MESH:D006969|MESH:D012873|MESH:D017443
TreeNumbers:C16.320.850.210 |C17.800.174.193 |C17.800.815.193 |C17.800.827.210 |C20.543.480.343
Synonyms:Atopic Dermatitides |Atopic Dermatitis |Atopic Eczema |Atopic Neurodermatitides |Atopic Neurodermatitis |Dermatitides, Atopic |Disseminated Neurodermatitides |Disseminated Neurodermatitis |Eczema, Atopic |Eczema, Infantile |Infantile Eczema |Neurodermatitides, Atop
Slim Mappings:Genetic disease (inborn)|Immune system disease|Skin disease
Reference: MedGen: D003876
MeSH: D003876
OMIM: 603165;

Genes:
Phenotypes
1 HP:0000006Autosomal dominant inheritance
2 HP:0001939Abnormality of metabolism/homeostasis
3 HP:0003193Allergic rhinitis
4 HP:0002099Asthma
5 HP:0001047Atopic dermatitis
6 HP:0000518Cataract
7 HP:0000509Conjunctivitis
8 HP:0000958Dry skin
9 HP:0000964Eczema
10 HP:0001041Facial erythema
11 HP:0007453Flexural lichenification
12 HP:0012537Food intolerance
13 HP:0008064Ichthyosis
14 HP:0011232Infra-orbital fold
15 HP:0000563Keratoconus
16 HP:0000980Pallor
17 HP:0000989Pruritus
18 HP:0001581Recurrent skin infections
Disease Causing ClinVar Variants