modern wellness · Symptom
Skin rash
🩺 HPO Source
🔤 Synonyms (2)
Synonyms
RashSkin rash
🔗 Cross-References (4)
MEDDRA10037844
SNOMEDCT_US112625008
SNOMEDCT_US271807003
UMLSC0015230
🔼 Broader Terms (1)
HP:0011123Inflammatory abnormality of the skin
🏥 Conditions where Skin rash appears
40 · bridged via HPO ↔ OMIM
syndrome OMIM 615846
Aicardi-Goutieres Syndrome 7
freq: 1/5 ev: PCS
syndrome OMIM 105200
Amyloidosis, Familial Visceral
ev: TAS
syndrome OMIM 616050
Autoinflammation With Infantile Enterocolitis
freq: 1/3 ev: PCS
syndrome OMIM 616744
Autoinflammatory Syndrome, Familial, Behcet-Like
freq: 4/11 ev: PCS
syndrome OMIM 158810
Bethlem Myopathy 1
freq: 0/1 ev: PCS
syndrome OMIM 253260
Biotinidase Deficiency
freq: 21/31 ev: PCS
syndrome OMIM 607115
Chronic Infantile Neurological, Cutaneous, And Articular Syndrome
freq: 3/3 onset: HP:0003577 ev: PCS
syndrome OMIM 607115
Chronic Infantile Neurological, Cutaneous, And Articular Syndrome
freq: 8/8 ev: PCS
syndrome OMIM 612714
Exocrine Pancreatic Insufficiency, Dyserythropoietic Anemia, And Calvarial Hyperostosis
freq: 3/5 ev: PCS
syndrome OMIM 120100
Familial Cold Autoinflammatory Syndrome 1
ev: PCS
syndrome OMIM 611762
Familial Cold Autoinflammatory Syndrome 2
ev: TAS
syndrome OMIM 120100
Familial Cold Urticaria
ev: PCS
syndrome OMIM 603553
Hemophagocytic Lymphohistiocytosis, Familial, 2
freq: 22/84 ev: PCS
syndrome OMIM 603552
Hemophagocytic Lymphohistiocytosis, Familial, 4
freq: 5/14 ev: PCS
syndrome OMIM 253270
Holocarboxylase Synthetase Deficiency
ev: IEA
syndrome OMIM 147060
Hyper-Ige Recurrent Infection Syndrome 1, Autosomal Dominant
freq: 37/57 onset: HP:0003623 ev: PCS
syndrome OMIM 147060
Hyper-Immunoglobulin E Syndrome, Autosomal Dominant
freq: 37/57 onset: HP:0003623 ev: PCS
syndrome OMIM 260920
Hyperimmunoglobulinemia D
freq: 20/20 ev: PCS
syndrome OMIM 256500
Ichthyosis Linearis Circumflexa
freq: 2/2 ev: PCS
syndrome OMIM 615468
Immunodeficiency 12
freq: 1/1 ev: PCS
syndrome OMIM 617585
Immunodeficiency 53
freq: 1/3 ev: PCS
syndrome OMIM 618108
Immunodeficiency 57
freq: 1/4 ev: PCS
syndrome OMIM 612852
Interleukin 1 Receptor Antagonist Deficiency
freq: 1/1 ev: PCS
syndrome OMIM 609628
Majeed Syndrome
freq: 2/6 ev: PCS
disease OMIM 617600
Mental Retardation, Autosomal Dominant 45
freq: 1/5 ev: PCS
syndrome OMIM 277380
Methylmalonic Aciduria And Homocystinuria, Cblf Type (Disorder)
freq: 1/12 ev: PCS
syndrome OMIM 610377
Mevalonic Aciduria
freq: 2/3 ev: PCS
syndrome OMIM 617523
Neurodevelopmental Disorder With Midbrain And Hindbrain Malformations
freq: 1/2 ev: PCS
syndrome OMIM 603554
Omenn Syndrome
freq: 1/1 ev: PCS
syndrome OMIM 617099
Otulin-Related Autoinflammatory Syndrome
freq: 3/3 ev: PCS
syndrome OMIM 102700
Partial Adenosine Deaminase Deficiency
freq: 1/1 ev: PCS
syndrome OMIM 617718
Platelet Abnormalities With Eosinophilia And Immune-Mediated Inflammatory Disease
freq: 3/3 ev: PCS
syndrome OMIM 604173
Poikiloderma With Neutropenia
freq: 3/3 ev: PCS
syndrome OMIM 615688
Polyarteritis Nodosa, Childhood-Onset
freq: 3/9 ev: PCS
syndrome OMIM 618048
Proteasome-Associated Autoinflammatory Syndrome 2
freq: 2/2 ev: PCS
syndrome OMIM 617591
Proteasome-Associated Autoinflammatory Syndrome 3
ev: IEA
syndrome OMIM 603554
Reticuloendotheliosis, Familial, With Eosinophilia
freq: 1/1 ev: PCS
syndrome OMIM 102700
Scid Due To Ada Deficiency, Early-Onset
freq: 1/1 ev: PCS
syndrome OMIM 102700
Severe Combined Immunodeficiency Due To Adenosine Deaminase Deficiency
freq: 1/1 ev: PCS
syndrome OMIM 270150
Sicca Syndrome
freq: 20/60 ev: PCS