Lymphoma, and Anxiety

Diseases related with Lymphoma and Anxiety

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

Top matches:

Celiac disease, also known as celiac sprue and gluten-sensitive enteropathy (GSE), is a multifactorial disorder of the small intestine that is influenced by both environmental and genetic factors. It is characterized by malabsorption resulting from inflammatory injury to the mucosa of the small intestine after the ingestion of wheat gluten or related rye and barley proteins (summary by Farrell and Kelly, 2002). Long regarded as gastrointestinal disorder of childhood, the disease is now considered to be a chronic systemic autoimmune disease and is more often diagnosed in adults than in children (Monsuur et al., 2005).For a discussion of genetic heterogeneity of celiac disease, see MAPPING.

CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1 Is also known as celiac sprue, susceptibility to, 1|gluten-sensitive enteropathy, susceptibility to, 1

Related symptoms:

  • Seizures
  • Short stature
  • Ataxia
  • Failure to thrive
  • Anemia


SOURCES: OMIM MENDELIAN

More info about CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1

Growth delay due to IGF-I resistance is characterised by variable intrauterine and postnatal growth retardation and elevated serum IGF-I levels. Addition features include variable degrees of intellectual deficit, microcephaly and dysmorphism (broad nasal bridge and tip, smooth philtrum, thin upper and everted lower lips, short fingers, clinodactyly, wide-set nipples and pectus excavatum).

GROWTH DELAY DUE TO INSULIN-LIKE GROWTH FACTOR I RESISTANCE Is also known as igf-i resistance|resistance to igf-1|somatomedin, end-organ insensitivity to|somatomedin-c, resistance to

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Short stature
  • Generalized hypotonia
  • Microcephaly


SOURCES: ORPHANET OMIM MENDELIAN

More info about GROWTH DELAY DUE TO INSULIN-LIKE GROWTH FACTOR I RESISTANCE

Pitt-Hopkins syndrome (PHS) is characterized by the association of intellectual deficit, characteristic facial dysmorphism and problems of abnormal and irregular breathing.

PITT-HOPKINS SYNDROME Is also known as encephalopathy, severe epileptic, with autonomic dysfunction|mental retardation, syndromal, with intermittent hyperventilation

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Hearing impairment


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about PITT-HOPKINS SYNDROME

Other less relevant matches:

Ataxia-telangiectasia is the association of severe combined immunodeficiency (affecting mainly the humoral immune response) with progressive cerebellar ataxia. It is characterised by neurological signs, telangiectasias, increased susceptibility to infections and a higher risk of cancer.

ATAXIA-TELANGIECTASIA Is also known as at1|louis-bar syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Short stature
  • Microcephaly
  • Scoliosis


SOURCES: ORPHANET OMIM MENDELIAN

More info about ATAXIA-TELANGIECTASIA

Machado-Joseph disease, named for affected families of Azorean extraction, is an autosomal dominant progressive neurologic disorder characterized principally by ataxia, spasticity, and ocular movement abnormalities. Although independently described as a seemingly separate disorder, spinocerebellar ataxia-3 is now known to be the same as Machado-Joseph disease.Three classic clinical subtypes of MJD are recognized: type 1 with early onset and marked pyramidal and dystonic signs; type 2, or pure, with predominant cerebellar ataxia; and type 3 with later-onset and peripheral neuropathy (Franca et al., 2008).

MACHADO-JOSEPH DISEASE; MJD Is also known as spinocerebellar ataxia 3|spinocerebellar atrophy iii|spinopontine atrophy|azorean neurologic disease|nigrospinodentatal degeneration|sca3

Related symptoms:

  • Ataxia
  • Nystagmus
  • Pain
  • Spasticity
  • Ptosis


SOURCES: OMIM MENDELIAN

More info about MACHADO-JOSEPH DISEASE; MJD

Usher syndrome is a clinically and genetically heterogeneous autosomal recessive disorder characterized by sensorineural hearing deficiencies at birth and later development of progressive retinitis pigmentosa (RP). It is the most frequent cause of combined deafness and blindness in adults and affects 3 to 6% of children born with hearing impairment. In brief, patients with Usher syndrome type II have mild hearing impairment with normal vestibular responses. Type II is the most common of the 3 Usher syndromes (Eudy et al., 1998). See {276900} for clinical characterization of Usher syndrome types I, II, and III. Genetic Heterogeneity of Usher Syndrome Type IIUsher syndrome type II is genetically heterogeneous. USH2C (OMIM ) can be caused by mutation in the ADGRV1 gene (OMIM ) or by biallelic digenic mutation in the ADGRV1 and PDZD7 (OMIM ) genes. USH2D (OMIM ) is caused by mutation in the WHRN gene (OMIM ).The locus designation USH2B has been withdrawn; see HISTORY.

Related symptoms:

  • Hearing impairment
  • Sensorineural hearing impairment
  • Blindness
  • Depressivity
  • Rod-cone dystrophy


SOURCES: OMIM MENDELIAN

More info about USHER SYNDROME, TYPE IIA; USH2A

Punctate palmoplantar keratoderma type I (PPKP1), also known as Buschke-Fischer-Brauer syndrome, is a very rare hereditary skin disease characterized by irregularly distributed epidermal hyperkeratosis of the palms and soles with wide variation among patients..

PUNCTATE PALMOPLANTAR KERATODERMA TYPE 1 Is also known as palmoplantar keratoderma, punctate type i|ppkp1|keratodermia palmoplantaris papulosa, buschke-fischer-brauer type|buschke-fischer-brauer syndrome|keratosis palmoplantaris papulosa|kppp1

Related symptoms:

  • Neoplasm
  • Pain
  • Dilatation
  • Depressivity
  • Hyperkeratosis


SOURCES: ORPHANET OMIM MENDELIAN

More info about PUNCTATE PALMOPLANTAR KERATODERMA TYPE 1

Neurofibromatosis type I is an autosomal dominant disorder characterized by cafe-au-lait spots, Lisch nodules in the eye, and fibromatous tumors of the skin. Individuals with the disorder have increased susceptibility to the development of benign and malignant tumors. NF1 is sometimes referred to as 'peripheral neurofibromatosis.' The worldwide incidence of NF1 is 1 in 2,500 to 1 in 3,000 individuals (reviews by Shen et al., 1996 and Williams et al., 2009).Type II neurofibromatosis (NF2 ) is a genetically distinct disorder caused by mutation in the gene encoding merlin (NF2 ) on chromosome 22q12. NF2, sometimes known as 'central neurofibromatosis,' is characterized by bilateral acoustic neuroma and meningioma, but few skin lesions or neurofibromas (Rouleau et al., 1993).Some patients with homozygous or compound heterozygous mutations in mismatch repair genes (see, e.g., MLH1; {120436} and MSH2; {609309}) have a phenotype characterized by early onset malignancies and mild features of NF1, especially cafe-au-lait spots; this is known as the mismatch repair cancer syndrome (OMIM ), sometimes referred to as brain tumor-polyposis syndrome-1 or Turcot syndrome. These patients typically do not have germline mutations in the NF1 gene, although a study by Wang et al. (2003) suggested that biallelic mutations in mismatch repair genes may cause somatic mutations in the NF1 gene, perhaps resulting in isolated features resembling NF1.See also Legius syndrome (OMIM ), a genetically distinct disorder with a similar phenotype to NF1.

NEUROFIBROMATOSIS TYPE 1 DUE TO NF1 MUTATION OR INTRAGENIC DELETION Is also known as von recklinghausen disease due to nf1 mutation or intragenic deletion|neurofibromatosis, peripheral type|von recklinghausen disease

Related symptoms:

  • Intellectual disability
  • Seizures
  • Short stature
  • Scoliosis
  • Hypertelorism


SOURCES: ORPHANET OMIM MENDELIAN

More info about NEUROFIBROMATOSIS TYPE 1 DUE TO NF1 MUTATION OR INTRAGENIC DELETION

MAJOR DEPRESSIVE DISORDER; MDD Is also known as unipolar depression

Related symptoms:

  • Neoplasm
  • Behavioral abnormality
  • Depressivity
  • Anxiety
  • Abnormality of the liver


SOURCES: OMIM MENDELIAN

More info about MAJOR DEPRESSIVE DISORDER; MDD

PARAGANGLIOMAS 3; PGL3 Is also known as glomus tumors, familial, 3

Related symptoms:

  • Hyperhidrosis
  • Tachycardia
  • Palpitations
  • Hoarse voice
  • Cranial nerve paralysis


SOURCES: OMIM MENDELIAN

More info about PARAGANGLIOMAS 3; PGL3

Top 5 symptoms//phenotypes associated to Lymphoma and Anxiety

Symptoms // Phenotype % cases
Depressivity Common - Between 50% and 80% cases
Seizures Uncommon - Between 30% and 50% cases
Ataxia Uncommon - Between 30% and 50% cases
Failure to thrive Uncommon - Between 30% and 50% cases
Hodgkin lymphoma Uncommon - Between 30% and 50% cases

Other less frequent symptoms

Patients with Lymphoma and Anxiety. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases

Neoplasm Short stature Intellectual disability Multiple cafe-au-lait spots Leukemia Gait ataxia Microcephaly Scoliosis Abnormal facial shape Dysarthria Peripheral neuropathy Strabismus Polyneuropathy Truncal ataxia Cafe-au-lait spot Postnatal growth retardation Breast carcinoma Anemia Diabetes mellitus Cognitive impairment Pain

Rare Symptoms - Less than 30% cases

Autism Specific learning disability Renal cell carcinoma Neurological speech impairment Autistic behavior Behavioral abnormality Finger clinodactyly Deeply set eye Paraganglioma Small hand Hypertelorism Wide intermamillary distance Type II diabetes mellitus Hearing impairment Epidermal acanthosis Aganglionic megacolon Abnormality of the skeletal system Spasticity Dilatation Abnormality of eye movement Absent Achilles reflex Spinocerebellar tract degeneration Chronic myelogenous leukemia Ptosis Visual impairment Spinal muscular atrophy Limb ataxia Progressive cerebellar ataxia Abnormal cerebellum morphology Distal amyotrophy Unsteady gait Abnormality of the liver Abnormal autonomic nervous system physiology Carcinoma Myoclonus Back pain Dystonia Cerebellar atrophy Tremor Skeletal muscle atrophy Flexion contracture Clinodactyly Nystagmus Blindness Incoordination Upslanted palpebral fissure Pneumonia Osteoporosis Hypoplasia of the corpus callosum Weight loss Wide nasal bridge Motor delay Malabsorption Delayed puberty Delayed speech and language development Abdominal distention IgA deficiency Growth delay Elevated hepatic transaminase Generalized hypotonia Global developmental delay Fatigue Decreased number of peripheral myelinated nerve fibers Brow ptosis Gaze-evoked nystagmus Atrophy/Degeneration affecting the brainstem Progressive external ophthalmoplegia Amyotrophic lateral sclerosis Fibular bowing Alcoholism Stroke Impaired vibratory sensation Schizophrenia Bipolar affective disorder Delusions Mania Agoraphobia Suicidal ideation Akinesia Hyperhidrosis Tachycardia Ophthalmoparesis Urinary bladder sphincter dysfunction Low back pain Spastic dysarthria Tibial pseudoarthrosis Progressive hearing impairment Bilateral sensorineural hearing impairment Pigmentary retinopathy Cerebral artery stenosis Nyctalopia Retinopathy Rod-cone dystrophy Sensorineural hearing impairment Abnormal electrooculogram Facial-lingual fasciculations Palatal myoclonus Impaired horizontal smooth pursuit Tongue fasciculations Downbeat nystagmus Supranuclear ophthalmoplegia Delirium Dysmetric saccades Restless legs Hypometric saccades Torsion dystonia Chronic pain Dilated fourth ventricle External ophthalmoplegia Myokymia Olivopontocerebellar atrophy Palpitations Vocal cord paralysis Hoarse voice Mucosal telangiectasiae Optic atrophy Chemodectoma Extraadrenal pheochromocytoma Defective B cell differentiation IgE deficiency Interosseus muscle atrophy Decreased/absent ankle reflexes Immunoglobulin IgG2 deficiency Progressive spinal muscular atrophy Non-Hodgkin lymphoma Aplasia/Hypoplasia of the thymus Hypertension associated with pheochromocytoma Increased sensitivity to ionizing radiation Female hypogonadism Chronic hepatitis Decreased proportion of CD4-positive T cells Elevated alpha-fetoprotein Abnormal spermatogenesis Neoplasm of the breast Glomus jugular tumor Conjunctival telangiectasia Loss of voice Dysphagia Babinski sign Fasciculations Gliosis Cranial nerve paralysis Hallucinations Vestibular dysfunction Diplopia Recurrent paroxysmal headache Abnormality of extrapyramidal motor function Adrenal pheochromocytoma Pulsatile tinnitus Bradykinesia Neuronal loss in central nervous system Parkinsonism Dementia Muscle cramps Postural instability Neurodegeneration Episodic paroxysmal anxiety Sensory neuropathy Confusion Ophthalmoplegia Abnormal pyramidal sign Abnormality of the eye Rigidity Proptosis Congenital sensorineural hearing impairment Arterial fibromuscular dysplasia Severe hearing impairment Sarcoma Renal artery stenosis Severe vision loss Osteomalacia Freckling Tibial bowing Neurofibromas Pulmonary fibrosis Hypophosphatemia Sensory axonal neuropathy Clitoral hypertrophy Precocious puberty Reduced bone mineral density Overweight Renovascular hypertension Venous thrombosis Atherosclerosis Spina bifida Sensorimotor neuropathy Bone pain Hypsarrhythmia Coarctation of aorta Mitral valve prolapse Abnormality of the cardiovascular system Tetralogy of Fallot Single ventricle Increased reactive oxygen species production Gastrointestinal hemorrhage Soft tissue sarcoma Leiomyosarcoma Neoplasm of the central nervous system Lisch nodules Dural ectasia Epigastric pain Renal phosphate wasting Schwannoma Glioma Nasolacrimal duct obstruction Rhabdomyosarcoma Carcinoid tumor Night sweats Gangrene Anomalous pulmonary venous return Complete atrioventricular canal defect Pheochromocytoma Pseudoarthrosis Parathyroid adenoma Aqueductal stenosis Astrocytoma Brain neoplasm Myocardial fibrosis Neoplasm of the endocrine system Meningioma Overgrowth Recurrent fractures Severe sensorineural hearing impairment Scaling skin Macrocephaly Hypertension Optic nerve glioma Transitional cell carcinoma of the bladder Orthokeratosis Hypergranulosis Neoplasm of the pancreas Parakeratosis Subcutaneous neurofibromas Colon cancer Squamous cell carcinoma Abnormality of the nail Neurofibrosarcoma Thickened skin Acute promyelocytic leukemia Abnormality of the skin Palmoplantar keratoderma Papule Hyperkeratosis Plexiform neurofibroma Inguinal freckling Spinal neurofibromas Gastrointestinal stroma tumor Mild hearing impairment Respiratory insufficiency Hydrocephalus Abnormality of skin pigmentation Osteopenia Peripheral axonal neuropathy Paresthesia Facial asymmetry Genu valgum Axillary freckling Pulmonic stenosis Pruritus Attention deficit hyperactivity disorder Paralysis Hypertrophic cardiomyopathy Hypoglycemia Cellular immunodeficiency Cardiomyopathy Kyphoscoliosis Glaucoma Embryonal rhabdomyosarcoma Vestibular Schwannoma Hyperactivity Abnormal heart morphology Visual loss Abnormality of cardiovascular system morphology Headache Intellectual disability, mild Neuroma Abnormality of chromosome stability Telangiectasia Chronic lymphatic leukemia Decreased body weight Truncal obesity Delayed cranial suture closure High pitched voice Agitation Radial deviation of finger Lipodystrophy Patent foramen ovale Pterygium Acanthosis nigricans Sandal gap Accelerated skeletal maturation Sparse scalp hair Severe intrauterine growth retardation Blue sclerae Webbed neck Broad nasal tip Triangular face Delayed eruption of teeth Short foot Highly arched eyebrow Everted lower lip vermilion Inability to walk Short distal phalanx of finger Short palm Reduced subcutaneous adipose tissue Severe failure to thrive Smooth philtrum Feeding difficulties Micropenis Pes cavus Constipation Encephalopathy Absent speech Intellectual disability, severe Short neck Anteverted nares Talipes equinovarus Myopia Depressed nasal bridge Cryptorchidism Maternal diabetes Muscular hypotonia Increased serum insulin-like growth factor 1 Burkitt lymphoma Hypoplastic facial bones Prominent scalp veins Rieger anomaly Broad finger Esodeviation Perimembranous ventricular septal defect Abnormality of the rib cage Small face Thin vermilion border Synophrys Gastroesophageal reflux Hypoplasia of dental enamel Macrocytic anemia Celiac disease Steatorrhea Malnutrition Abnormality of the coagulation cascade Rickets Abnormal intestine morphology Spontaneous abortion Type I diabetes mellitus Hypocalcemia Chronic diarrhea Inflammatory abnormality of the skin Iron deficiency anemia Eczema Cerebral calcification Nevus Infertility Autoimmunity Irritability Arthralgia Abdominal pain Alopecia Diarrhea Vomiting Thyroiditis Thrombocytosis Small for gestational age Ventricular septal defect Muscular hypotonia of the trunk Thin upper lip vermilion Retrognathia Narrow mouth Severe short stature Delayed skeletal maturation Pectus excavatum Obesity Malar flattening Long philtrum Hypertonia Intrauterine growth retardation Chronic fatigue High palate Low-set ears Micrognathia Vitamin B12 deficiency Vitamin K deficiency Vitamin D deficiency Folate deficiency Abnormality of the abdominal wall Prolonged prothrombin time Recurrent aphthous stomatitis Stomatitis Prolonged partial thromboplastin time Mandibular prognathia Coarse facial features Hypoplasia of the thymus Distal muscle weakness Abnormal vertebral morphology Sinusitis Bronchiectasis Choreoathetosis Intention tremor Pancytopenia Apraxia Hepatitis Decreased antibody level in blood Chorea Abnormality of movement Respiratory tract infection Abnormality of the hair Difficulty walking Recurrent respiratory infections Recurrent infections Immunodeficiency Gait disturbance Muscle weakness Overhanging nasal tip Triangular nasal tip Broad fingertip Intermittent hyperventilation Narrow foot Lymphopenia Recurrent pneumonia Small cerebral cortex Prematurely aged appearance Lymphoproliferative disorder Abnormality of the testis B-cell lymphoma Renal neoplasm Recurrent bronchitis Chromosome breakage Recurrent lower respiratory tract infections Severe combined immunodeficiency Acute lymphoblastic leukemia Hepatocellular carcinoma Hypopigmentation of hair Myeloid leukemia Oculomotor apraxia Abnormality of the immune system Telangiectasia of the skin Aplasia/Hypoplasia of the skin Resting tremor Premature graying of hair Combined immunodeficiency Glucose intolerance Athetosis Polycystic ovaries Slurred speech Cerebral palsy Reduced tendon reflexes Failure of eruption of permanent teeth Square face Pes planus Tapered finger Postnatal microcephaly Open mouth Thick lower lip vermilion Narrow forehead Cyanosis Convex nasal ridge Prominent nose Full cheeks Hypopigmentation of the skin Sleep disturbance Single transverse palmar crease Thick vermilion border Abnormal palate morphology Thick eyebrow Astigmatism Severe global developmental delay Prominent nasal bridge Short philtrum Wide mouth Protruding ear Abnormality of the pinna Apnea Intellectual disability, moderate Aggressive behavior Intellectual disability, progressive Widely spaced teeth Large beaked nose Hiatus hernia Happy demeanor Pes valgus Abnormal pattern of respiration Thickened helices Breathing dysregulation Abnormality of the helix Clubbing of fingers Echolalia Misalignment of teeth Esophagitis Acrocyanosis Hyperventilation Aplasia/Hypoplasia of the corpus callosum Dysphasia Aphasia Supernumerary nipple Overlapping toe Cupped ear Clubbing Self-injurious behavior Short metatarsal Coarse hair Hypopigmented skin patches Mutism Sleep apnea Elevated circulating catecholamine level


If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Melanoma and Atrial fibrillation, related diseases and genetic alterations Wide nasal bridge and Pancytopenia, related diseases and genetic alterations