Pain, and Atopic dermatitis

Diseases related with Pain and Atopic dermatitis

In the following list you will find some of the most common rare diseases related to Pain and Atopic dermatitis that can help you solving undiagnosed cases.

Top matches:

Related symptoms:

  • Fever
  • Hyperkeratosis
  • Arthralgia
  • Arthritis
  • Ichthyosis


SOURCES: OMIM MENDELIAN

More info about PSORIASIS 2; PSORS2

Infantile-onset multisystem autoimmune disease-1 is characterized by early childhood onset of a spectrum of autoimmune disorders affecting multiple organs. Common manifestations include insulin-dependent diabetes mellitus and autoimmune enteropathy, or celiac disease, and autoimmune hematologic disorders. Other features include short stature and nonspecific dermatitis. More variable features include hypothyroidism, autoimmune arthritis, and delayed puberty. Some patients may show recurrent infections. The disorder results from an inborn error of cytokine signaling (summary by Flanagan et al., 2014 and Milner et al., 2015). Genetic Heterogeneity of Infantile-Onset Multisystem Autoimmune DiseaseSee also ADMIO2 (OMIM ), caused by mutation in the ZAP70 gene (OMIM ) on chromosome 2q12.

Related symptoms:

  • Short stature
  • Pain
  • Anemia
  • Abnormality of the dentition
  • Immunodeficiency


SOURCES: OMIM ORPHANET MENDELIAN

More info about STAT3-RELATED EARLY-ONSET MULTISYSTEM AUTOIMMUNE DISEASE

Bronchial asthma is the most common chronic disease affecting children and young adults. It is a complex genetic disorder with a heterogeneous phenotype, largely attributed to the interactions among many genes and between these genes and the environment.Asthma-related traits include clinical symptoms of asthma, such as coughing, wheezing, and dyspnea; bronchial hyperresponsiveness (BHR) as assessed by methacholine challenge test; serum IgE levels; atopy; and atopic dermatitis (Laitinen et al., 2001; Illig and Wjst, 2002; Pillai et al., 2006). See {147050} for information on the asthma-associated phenotype atopy.

ASTHMA, SUSCEPTIBILITY TO Is also known as asthma, bronchial|asthma-related traits, susceptibility to

Related symptoms:

  • Fever
  • Respiratory distress
  • Dyspnea
  • Cough
  • Asthma


SOURCES: OMIM MENDELIAN

More info about ASTHMA, SUSCEPTIBILITY TO

Other less relevant matches:

Dyschromatosis universalis hereditaria (DUH) is a rare autosomal dominant genodermatosis characterized by irregularly shaped asymptomatic hyper- and hypopigmented macules that appear in infancy or early childhood and occur in a generalized distribution over the trunk, limbs, and sometimes the face. Involvement of the palms or soles is unusual. Abnormalities of hair and nails have been reported, and DUH may be associated with abnormalities of dermal connective tissue, nerve tissue, or other systemic complications (summary by Zhang et al., 2013).For a discussion of genetic heterogeneity of DUH, see DUH1 (OMIM ).

Related symptoms:

  • Neoplasm
  • Pain
  • Coloboma
  • Pruritus
  • Hypopigmentation of the skin


SOURCES: OMIM MENDELIAN

More info about DYSCHROMATOSIS UNIVERSALIS HEREDITARIA 3; DUH3

Low match MELAS

MELAS (Mitochondrial myopathy, encephalopathy, lactic acidosis, and stroke) syndrome is a rare progressive multisystemic disorder characterized by encephalomyopathy, lactic acidosis, and stroke-like episodes. Other features include endocrinopathy, heart disease, diabetes, hearing loss, and neurological and psychiatric manifestations.

MELAS Is also known as mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes|melas syndrome|mitochondrial myopathy, encephalopathy, lactic acidosis and stroke-like episodes

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Hearing impairment


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about MELAS

Asthma-related traits include clinical symptoms of asthma, such as coughing, wheezing, and dyspnea; bronchial hyperresponsiveness (BHR) as assessed by methacholine challenge test; serum IgE levels; atopy; and atopic dermatitis (Laitinen et al., 2001; Illig and Wjst, 2002; Pillai et al., 2006).For a general phenotypic description and a discussion of genetic heterogeneity of asthma, see {600807}.

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1 Is also known as as1|asrt1

Related symptoms:

  • Dyspnea
  • Cough
  • Asthma
  • Inflammatory abnormality of the skin
  • Wheezing


SOURCES: OMIM MENDELIAN

More info about ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 1

Asthma-related traits include clinical symptoms of asthma, such as coughing, wheezing, and dyspnea; bronchial hyperresponsiveness (BHR) as assessed by methacholine challenge test; serum IgE levels; atopy; and atopic dermatitis (Laitinen et al., 2001; Illig and Wjst, 2002).For a general phenotypic description and a discussion of genetic heterogeneity of asthma, see {600807}.

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 2 Is also known as asrt2

Related symptoms:

  • Dyspnea
  • Cough
  • Asthma
  • Inflammatory abnormality of the skin
  • Wheezing


SOURCES: OMIM MENDELIAN

More info about ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 2

Asthma-related traits include clinical symptoms of asthma, such as coughing, wheezing, and dyspnea; bronchial hyperresponsiveness (BHR) as assessed by methacholine challenge test; serum IgE levels; atopy; and atopic dermatitis (Laitinen et al., 2001; Illig and Wjst, 2002; Pillai et al., 2006).For a general phenotypic description and a discussion of genetic heterogeneity of asthma, see {600807}.

ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 5 Is also known as asrt5

Related symptoms:

  • Dyspnea
  • Cough
  • Asthma
  • Inflammatory abnormality of the skin
  • Wheezing


SOURCES: OMIM MENDELIAN

More info about ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 5

Asthma-related traits include clinical symptoms of asthma, such as coughing, wheezing, and dyspnea; bronchial hyperresponsiveness (BHR) as assessed by methacholine challenge test; serum IgE levels; atopy; and atopic dermatitis (Laitinen et al., 2001; Illig and Wjst, 2002; Pillai et al., 2006).For a general phenotypic description and a discussion of genetic heterogeneity of asthma, see {600807}.

Related symptoms:

  • Dyspnea
  • Cough
  • Asthma
  • Inflammatory abnormality of the skin
  • Wheezing


SOURCES: OMIM MENDELIAN

More info about ASTHMA-RELATED TRAITS, SUSCEPTIBILITY TO, 7; ASRT7

Inflammation of the mucous membrane lining the nose due to allergy.

ALLERGIC RHINITIS Is also known as alrh

Related symptoms:

  • Asthma
  • Inflammatory abnormality of the skin
  • Rhinitis
  • Atopic dermatitis
  • Allergy


SOURCES: OMIM MENDELIAN

More info about ALLERGIC RHINITIS

Top 5 symptoms//phenotypes associated to Pain and Atopic dermatitis

Symptoms // Phenotype % cases
Inflammatory abnormality of the skin Common - Between 50% and 80% cases
Asthma Common - Between 50% and 80% cases
Dyspnea Common - Between 50% and 80% cases
Wheezing Uncommon - Between 30% and 50% cases
Cough Uncommon - Between 30% and 50% cases

Other less frequent symptoms

Patients with Pain and Atopic dermatitis. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases

Fever

Rare Symptoms - Less than 30% cases

Pruritus Allergic rhinitis Type I diabetes mellitus Eczema Delayed puberty Hypothyroidism Diabetes mellitus Abnormality of the dentition Respiratory distress Anemia Ichthyosis Short stature Arthritis Arthralgia Hemiparesis Hemiplegia Intestinal obstruction Personality changes Ophthalmoparesis Hyponatremia Abnormality of mitochondrial metabolism Aortic aneurysm Bilateral ptosis Bifid scrotum Hypercalciuria Decreased nerve conduction velocity Cachexia Atrioventricular block Chronic kidney disease Growth abnormality Easy fatigability Aplasia/Hypoplasia of the cerebellum Mask-like facies Goiter Hyperkalemia Basal ganglia calcification Glomerulopathy Progressive sensorineural hearing impairment Vertebral fusion Multiple lipomas Prolonged QT interval Visual field defect Dysphasia Hemiplegia/hemiparesis Vestibular dysfunction Aphasia Bundle branch block Adrenal insufficiency Overlapping toe Abnormality of neuronal migration Focal segmental glomerulosclerosis Hyperkinesis Schizophrenia Hypertrichosis Abnormality of retinal pigmentation Bilateral sensorineural hearing impairment Cardiac arrest Clonus Nephrotic syndrome Cerebral visual impairment Hallucinations Gingival overgrowth EMG abnormality Type II diabetes mellitus Anorexia Left ventricular hypertrophy Decreased body weight Involuntary movements Pulmonary arterial hypertension Status epilepticus Truncal ataxia Generalized hirsutism Mutism Abnormality of the cardiovascular system Psychosis Hypopigmented skin patches Ischemic stroke Ragged-red muscle fibers Ventricular hypertrophy Atrial fibrillation Pigmentary retinopathy Generalized-onset seizure Hypogonadotrophic hypogonadism Rhabdomyolysis Reduced tendon reflexes External ophthalmoplegia Pancreatitis Macular degeneration Purpura Exercise intolerance Hyperthyroidism Heart block Thyroiditis Amaurosis fugax Crohn's disease Abnormality of the cerebellar vermis Psychotic episodes Tubulointerstitial abnormality Renal Fanconi syndrome Abnormal nerve conduction velocity Auditory hallucinations Gastroparesis Abnormal macular morphology Spontaneous hematomas Leber optic atrophy Persistence of primary teeth Writer's cramp Muscle fiber atrophy Psychomotor deterioration Dysesthesia Hemeralopia Spotty hypopigmentation Episodic vomiting Homonymous hemianopia Rhinitis Prominent ear helix Morphological abnormality of the inner ear Morphological abnormality of the vestibule of the inner ear Bilateral intracranial calcifications Episodic quadriplegia Abnormality of acid-base homeostasis Abnormal cochlea morphology Paronychia Paralytic ileus Abnormal mitochondrial shape Cochlear degeneration Progressive night blindness Cochlear malformation Edema of the dorsum of hands Abnormal mitochondrial morphology Motor polyneuropathy Abnormality of the renal tubule Abnormality of immune system physiology Xerostomia Delusions Transient ischemic attack Posterior subcapsular cataract Progressive external ophthalmoplegia Mitochondrial myopathy Hypoparathyroidism Amenorrhea Vitiligo Facial diplegia Neonatal hypoglycemia Abnormality of visual evoked potentials Hashimoto thyroiditis Drowsiness Distal arthrogryposis Pulmonary embolism Primary adrenal insufficiency Cardiorespiratory arrest Aortic dissection Hemianopia Stroke-like episode Ileus Proximal tubulopathy Abnormality of peripheral nerve conduction Retinal pigment epithelial atrophy Speech apraxia Left ventricular failure Seborrheic dermatitis Anterior hypopituitarism Renal tubular dysfunction Gait imbalance Reduced consciousness/confusion Cerebral ischemia Wolff-Parkinson-White syndrome Increased CSF lactate Visual hallucinations Tubulointerstitial nephritis Cerebral calcification Coma Specific learning disability Sensorineural hearing impairment Visual impairment Feeding difficulties Cognitive impairment Ptosis Cataract Muscular hypotonia Muscle weakness Failure to thrive Hypertension Nystagmus Hypertelorism Growth delay Ataxia Microcephaly Hearing impairment Global developmental delay Motor delay Peripheral neuropathy Intellectual disability Ventriculomegaly Vomiting Cerebellar atrophy Myopathy Blindness Cardiomyopathy Short neck Respiratory insufficiency Dysphagia Hepatomegaly Fatigue Gait disturbance Tremor Optic atrophy Skeletal muscle atrophy Dysarthria Hyperreflexia Seizures Neoplasm of the skin Congestive heart failure Immunodeficiency Autoimmunity Respiratory tract infection Hepatosplenomegaly Recurrent respiratory infections Pneumonia Thrombocytopenia Recurrent infections Diffuse skin atrophy Lymphadenopathy Orthokeratosis Parakeratosis Rheumatoid arthritis Psoriasiform dermatitis Scaling skin Dermal atrophy Epidermal acanthosis Leukemia Hemolytic anemia Hypopigmentation of the skin Autoimmune hemolytic anemia Coloboma Neoplasm Chest tightness Interstitial pneumonitis Primary hypothyroidism Recurrent ear infections Autoimmune thrombocytopenia Scleroderma Neutropenia Celiac disease Colitis Interstitial pulmonary abnormality Abnormal intestine morphology Lymphopenia Abnormal lung morphology Decreased antibody level in blood Diarrhea Hypertonia Hip dysplasia Arthrogryposis multiplex congenita Dysmetria Anal atresia Malabsorption Nausea and vomiting Carious teeth Congenital cataract Ophthalmoplegia Lethargy Confusion Generalized tonic-clonic seizures Dilated cardiomyopathy Neurological speech impairment Stroke Attention deficit hyperactivity disorder Nyctalopia Abnormality of the liver Paresthesia Vertigo Protruding ear Muscle cramps Memory impairment Increased serum lactate Migraine Sensory impairment Sudden cardiac death Generalized myoclonic seizures Abnormal cerebellum morphology Postural instability Peripheral axonal neuropathy Hyperkeratosis Polyneuropathy Nephropathy Hirsutism Polymicrogyria Nausea Lactic acidosis Erythema Abnormality of the pinna Dystonia Areflexia Dementia Rod-cone dystrophy Cerebellar hypoplasia Constipation Delayed skeletal maturation Elevated serum creatine phosphokinase Hyporeflexia Arrhythmia Osteoporosis Visual loss Encephalopathy Depressivity Cerebral atrophy Headache Renal insufficiency Kyphosis Myoclonus Hypogonadism Developmental regression EEG abnormality Feeding difficulties in infancy Mental deterioration Apnea Hypertrophic cardiomyopathy Proteinuria Anxiety Myalgia Photophobia Abdominal pain Jaundice Gastroesophageal reflux Acidosis Autism Weight loss Gait ataxia Cerebral cortical atrophy Allergy


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