Lymphoma, and Recurrent urinary tract infections

Diseases related with Lymphoma and Recurrent urinary tract infections

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

Top matches:

Medium match WHIM SYNDROME

WHIM (warts, hypogammaglobulinemia, infections, and myelokathexis) syndrome is a congenital autosomal dominant immune deficiency characterized by abnormal retention of mature neutrophils in the bone marrow (myelokathexis) and occasional hypogammaglobulinemia, associated with an increased risk for bacterial infections and a susceptibility to human papillomavirus (HPV) induced lesions (cutaneous warts, genital dysplasia and invasive mucosal carcinoma).

WHIM SYNDROME Is also known as warts, hypogammaglobulinemia, infections, and myelokathexis syndrome|warts-infections-leukopenia-myelokatexis syndrome|wilm|warts-hypogammaglobulinemia-infections-myelokathexis syndrome

Related symptoms:

  • Hearing impairment
  • Neoplasm
  • Fever
  • Congestive heart failure
  • Immunodeficiency


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about WHIM SYNDROME

Purine nucleoside phosphorylase (PNP) deficiency is a disorder of purine metabolism characterized by progressive immunodeficiency leading to recurrent and opportunistic infections, autoimmunity and malignancy as well as neurologic manifestations.

PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY Is also known as pnp deficiency|pnpase deficiency|nucleoside phosphorylase deficiency

Related symptoms:

  • Intellectual disability
  • Generalized hypotonia
  • Ataxia
  • Failure to thrive
  • Muscular hypotonia


SOURCES: ORPHANET OMIM MENDELIAN

More info about PURINE NUCLEOSIDE PHOSPHORYLASE DEFICIENCY

Medium match EEC SYNDROME

EEC syndrome is a genetic developmental disorder characterized by ectrodactyly, ectodermal dysplasia, and orofacial clefts (cleft lip/palate).

EEC SYNDROME Is also known as eec syndrome 3|ectrodactyly-ectodermal dysplasia-cleft lip/palate syndrome

Related symptoms:

  • Intellectual disability
  • Short stature
  • Hearing impairment
  • Sensorineural hearing impairment
  • Cleft palate


SOURCES: OMIM ORPHANET MENDELIAN

More info about EEC SYNDROME

Other less relevant matches:

Nijmegen breakage syndrome is a rare genetic disease presenting at birth with microcephaly, dysmorphic facial features, becoming more noticeable with age, growth delay, and later-onset complications such as malignancies and infections.

NIJMEGEN BREAKAGE SYNDROME Is also known as microcephaly-immunodeficiency-lymphoreticuloma syndrome|ataxia-telangiectasia variant v1|microcephaly with normal intelligence, immunodeficiency, and lymphoreticular malignancies|at-v1|berlin breakage syndrome|ataxia-telangiectasia, variant 1|seemanova sy

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Short stature
  • Microcephaly
  • Ataxia


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about NIJMEGEN BREAKAGE SYNDROME

Medium match ACHONDROPLASIA; ACH

Achondroplasia is the most frequent form of short-limb dwarfism. Affected individuals exhibit short stature caused by rhizomelic shortening of the limbs, characteristic facies with frontal bossing and midface hypoplasia, exaggerated lumbar lordosis, limitation of elbow extension, genu varum, and trident hand (summary by Bellus et al., 1995).

Related symptoms:

  • Intellectual disability
  • Short stature
  • Generalized hypotonia
  • Hearing impairment
  • Scoliosis


SOURCES: MESH OMIM MENDELIAN

More info about ACHONDROPLASIA; ACH

Low match FANCONI ANEMIA

Fanconi anemia (FA) is a hereditary DNA repair disorder characterized by progressive pancytopenia with bone marrow failure, variable congenital malformations and predisposition to develop hematological or solid tumors.

FANCONI ANEMIA Is also known as fanconi pancytopenia|fanconi anemia|fa

Related symptoms:

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


SOURCES: OMIM ORPHANET MENDELIAN

More info about FANCONI ANEMIA

Autosomal recessive severe congenital neutropenia due to CSF3R deficiency is a rare, genetic, primary immunodeficiency disorder characterized by predisposition to recurrent, life-threatening bacterial infections associated with decreased peripheral neutrophil granulocytes (absolute neutrophil count less than 500 cells/microliter), resulting from recessively inherited loss-of-function mutations in the CSF3R gene. Full maturation of all three lineages in the bone marrow and refractoriness to in vivo rhG-CSF treatment are associated.

Related symptoms:

  • Immunodeficiency
  • Recurrent infections
  • Pneumonia
  • Dyskinesia
  • Neutropenia


SOURCES: OMIM ORPHANET MENDELIAN

More info about AUTOSOMAL RECESSIVE SEVERE CONGENITAL NEUTROPENIA DUE TO CSF3R DEFICIENCY

Low match MIRAGE SYNDROME

MIRAGE syndrome is a form of syndromic adrenal hypoplasia, characterized by myelodysplasia, infection, restriction of growth, adrenal hypoplasia, genital phenotypes, and enteropathy. The condition is often fatal within the first decade of life, usually as a result of invasive infection (Narumi et al., 2016).

MIRAGE SYNDROME Is also known as myelodysplasia-infection-restriction of growth-adrenal hypoplasia-genital anomalies-enteropathy syndrome|myelodysplasia-infection-restriction of growth-adrenal hypoplasia-genital phenotypes-enteropathy syndrome|myelodysplasia, infection, restriction of gr

Related symptoms:

  • Seizures
  • Global developmental delay
  • Short stature
  • Scoliosis
  • Cryptorchidism


SOURCES: OMIM ORPHANET MENDELIAN

More info about MIRAGE SYNDROME

IMD50 is an X-linked recessive primary immunodeficiency characterized by the onset of recurrent bacterial or varicella zoster virus (VZV) infections in early childhood. Laboratory studies show profound lymphopenia, hypogammaglobulinemia, poor immune response to vaccine antigens, and fluctuating neutropenia. The disorder does not affect overall patient survival (summary by Lagresle-Peyrou et al., 2016).

COMBINED IMMUNODEFICIENCY DUE TO MOESIN DEFICIENCY Is also known as cid due to moesin deficiency|msn-related combined immunodeficiency|immunodeficiency 50, x-linked recessive|x-linked moesin-associated immunodeficiency

Related symptoms:

  • Immunodeficiency
  • Recurrent respiratory infections
  • Neutropenia
  • Decreased antibody level in blood
  • Eczema


SOURCES: OMIM ORPHANET MENDELIAN

More info about COMBINED IMMUNODEFICIENCY DUE TO MOESIN DEFICIENCY

X-linked immunodeficiency with magnesium defect, Epstein-Barr virus infection and neoplasia is a rare combined T and B cell immunodeficiency characterized by recurrent sinopulmonary and viral infections, persistent elevated Epstein-Barr virus (EBV) viremia and increased susceptibility to EBV-associated B-cell lymphoproliferative disorders. Immunological analyses show normal lymphocyte count or mild to moderate lymphopenia, inverted CD4:CD8 T-cell ratio and hypogammaglobulinemias.

X-LINKED IMMUNODEFICIENCY WITH MAGNESIUM DEFECT, EPSTEIN-BARR VIRUS INFECTION AND NEOPLASIA Is also known as combined immunodeficiency due to magt1 deficiency|cid due to magt1 deficiency|xmen

Related symptoms:

  • Neoplasm
  • Immunodeficiency
  • Recurrent infections
  • Lymphoma
  • Lymphopenia


SOURCES: ORPHANET OMIM MENDELIAN

More info about X-LINKED IMMUNODEFICIENCY WITH MAGNESIUM DEFECT, EPSTEIN-BARR VIRUS INFECTION AND NEOPLASIA

Top 5 symptoms//phenotypes associated to Lymphoma and Recurrent urinary tract infections

Symptoms // Phenotype % cases
Immunodeficiency Common - Between 50% and 80% cases
Short stature Uncommon - Between 30% and 50% cases
Neoplasm Uncommon - Between 30% and 50% cases
Intellectual disability Uncommon - Between 30% and 50% cases
Lymphopenia Uncommon - Between 30% and 50% cases

Other less frequent symptoms

Patients with Lymphoma and Recurrent urinary tract infections. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases

Neutropenia Otitis media Hearing impairment Pneumonia Hypospadias Global developmental delay Myelodysplasia B-cell lymphoma Motor delay Choanal atresia Growth delay Intrauterine growth retardation Ataxia Thrombocytopenia Depressed nasal bridge Cryptorchidism Leukemia Cleft palate Sinusitis Hydrocephalus Recurrent bacterial infections Scoliosis Anemia

Rare Symptoms - Less than 30% cases

Oral cleft External ear malformation Hydroureter Abnormality of femur morphology Renal hypoplasia/aplasia Severe short stature Renal agenesis Hearing abnormality Leukopenia Toe syndactyly Finger syndactyly Cleft lip Hydronephrosis Weight loss Malar flattening Gastroesophageal reflux Flexion contracture Myeloid leukemia Cleft upper lip Ventriculomegaly Hypergonadotropic hypogonadism Abnormality of the nervous system Abnormal eyelid morphology Cafe-au-lait spot Telangiectasia Chronic diarrhea Sloping forehead Patent ductus arteriosus Anal atresia Abnormality of chromosome stability Upslanted palpebral fissure Duplicated collecting system Recurrent respiratory infections Hyperreflexia Diarrhea Micrognathia Frontal bossing Abnormality of the skeletal system Microcephaly Neuroblastoma Small for gestational age Dysuria Failure to thrive Recurrent infections Generalized hypotonia Tetraparesis Combined immunodeficiency Recurrent upper respiratory tract infections Meningitis Bronchiectasis Decreased antibody level in blood Carious teeth Autoimmune hemolytic anemia Respiratory failure Congestive heart failure Recurrent viral infections Carcinoma Fever Delayed speech and language development Hyperkalemia Cataract Hepatomegaly Pes planus Epicanthus Hypertrophic cardiomyopathy Visual impairment High palate Ptosis Strabismus Abnormal facial shape Fatigue Achalasia Abnormality of the eye Intracranial hemorrhage Nystagmus Hypertelorism Microphallus Lumbar kyphosis in infancy Esophageal stricture Hyponatremia Umbilical hernia Respiratory distress Renal insufficiency Clinodactyly of the 5th finger Abnormal heart morphology Adrenal insufficiency Petechiae Abnormality of cardiovascular system morphology Shawl scrotum Headache Microphthalmia Adrenal hypoplasia Hypogonadism Rocker bottom foot Diabetes mellitus Spinal stenosis with reduced interpedicular distance Aspiration pneumonia Proptosis Overlapping fingers Atrial septal defect Hypothyroidism Myelitis Abnormal carotid artery morphology Trident hand Tibial bowing Osteopetrosis Megalencephaly Spinal cord compression Obstructive sleep apnea Abnormality of the elbow Spinal canal stenosis Hip contracture Disproportionate short stature Limited elbow extension Communicating hydrocephalus Bowel incontinence Short femoral neck Flared metaphysis Spondyloepiphyseal dysplasia Chronic otitis media Epiphyseal dysplasia Back pain Genu varum Abnormality of pelvic girdle bone morphology Generalized joint laxity Upper airway obstruction Radial club hand Neonatal short-limb short stature Limited hip extension Brain stem compression Childhood onset short-limb short stature Small foramen magnum Iritis Cervical cord compression Obstructive lung disease Cervical myelopathy Central sleep apnea Chronic myelogenous leukemia Central apnea Thoracolumbar kyphosis Recurrent ear infections Hypoplastic spleen Myelopathy Hypoxemia Multiple epiphyseal dysplasia Eczema Cor pulmonale Decreased proportion of CD4-positive T cells Hypopnea Irritability Abnormal intestine morphology Abnormality of the uterus Abnormal localization of kidney Abnormal renal morphology Abnormal aortic valve morphology Abnormality of the hypothalamus-pituitary axis Acute monocytic leukemia Dextrocardia Bicornuate uterus Abnormality of the thumb Abnormality of the testis Aplastic anemia Abnormal aortic morphology Abnormality of the upper limb Arteriovenous malformation Abnormality of the ulna Chromosome breakage Ciliary dyskinesia Irregular hyperpigmentation Aplasia/Hypoplasia of the radius Absent radius Abnormality of blood and blood-forming tissues Acute myeloid leukemia Reticulocytopenia Abnormality of nervous system morphology Absent thumb Decreased fertility in males Prolonged G2 phase of cell cycle Anemic pallor Deficient excision of UV-induced pyrimidine dimers in DNA Neoplasm of head and neck Aplasia/Hypoplasia of the uvula Compensated hypothyroidism Absent testis Aplasia/Hypoplasia of fingers Hypoplastic anemia Chromosomal breakage induced by crosslinking agents Clubbing of toes Primary hypothyroidism Pyridoxine-responsive sideroblastic anemia Abnormality of the preputium Partial duplication of thumb phalanx Complete duplication of thumb phalanx Aplasia/Hypoplasia of the iris Low-grade fever Meckel diverticulum Dyskinesia Aspiration Duodenal stenosis Multiple cafe-au-lait spots Ectopic kidney Abnormality of the kidney Facial asymmetry Short palpebral fissure Pancytopenia Oligohydramnios Tetralogy of Fallot Hypopigmentation of the skin Bruising susceptibility Abnormality of skin pigmentation Vertigo Astigmatism Abnormality of the foot Abnormality of the genital system Dolichocephaly Hip dislocation Abnormal cardiac septum morphology Sepsis Decreased testicular size Decreased body weight Abnormality of the liver Hyperpigmentation of the skin Postnatal growth retardation Almond-shaped palpebral fissure Paraplegia Aganglionic megacolon Squamous cell carcinoma Hypopigmented skin patches Congenital neutropenia Hypoplasia of the ulna Glucose intolerance Tracheoesophageal fistula Triphalangeal thumb Seizures Hyperinsulinemia Abnormality of the urinary system Abnormality of vision Reduced bone mineral density Disproportionate short-limb short stature Short thumb Cranial nerve paralysis Azoospermia Talipes equinovarus Type I diabetes mellitus Horseshoe kidney Bone marrow hypocellularity Hypoglycemia Spina bifida Abnormal vertebral morphology Insulin resistance Tinnitus Pain Short long bone Sparse scalp hair Cutaneous syndactyly Sparse eyelashes Abnormality of dental enamel Hypogonadotrophic hypogonadism Sparse and thin eyebrow Hypohidrosis Hypoplasia of dental enamel Renal dysplasia Split hand Fine hair Reduced number of teeth Microdontia Growth hormone deficiency Ectodermal dysplasia Vesicoureteral reflux Nevus Hypodontia Hypoplasia of the maxilla Thick eyebrow Dry skin Nail dystrophy Coarse hair Proximal placement of thumb Blepharophimosis Fair hair Slow-growing hair Entropion Lacrimation abnormality Anterior hypopituitarism Hypoplasia of the thymus Sparse pubic hair Sparse axillary hair Generalized hypopigmentation Corneal erosion Taurodontia Hypoplastic toenails Blue irides Depressed nasal tip Split foot Xerostomia Blepharitis Ectrodactyly Hypoplastic nipples Aplasia/Hypoplasia of the thumb Aplasia/Hypoplasia of the skin Keratitis Microtia Sparse hair Bladder diverticulum Abnormality of bone marrow cell morphology Tremor Spasticity Muscular hypotonia Myelokathexis Bone marrow hypercellularity Hypersegmentation of neutrophil nuclei Tonsillitis Septic arthritis Folliculitis Abnormality of female external genitalia Splenomegaly Abnormality of female internal genitalia Atelectasis Verrucae Periodontitis IgG deficiency Cellulitis Osteomyelitis Leukocytosis Respiratory tract infection Arthritis Behavioral abnormality Babinski sign Photophobia Recurrent opportunistic infections Micropenis Hyperkeratosis Polydactyly Dilatation Syndactyly Sensorineural hearing impairment Abnormality of B cell physiology Lymph node hypoplasia Brain abscess Cerebral vasculitis Abnormal T cell morphology Abnormal pyramidal sign Autoimmune neutropenia Pure red cell aplasia Hypouricemia Impaired T cell function Recurrent lower respiratory tract infections Autoimmune thrombocytopenia Spastic diplegia Spastic tetraparesis Spastic tetraplegia Tetraplegia Aplasia/Hypoplasia of the nipples Inflammatory abnormality of the eye Infantile muscular hypotonia Penoscrotal hypospadias Obesity Midface retrusion Macrocephaly Brachydactyly Hypertension Progressive vitiligo Mastoiditis Malar prominence Dysgammaglobulinemia Anorectal anomaly Arthralgia Recurrent infection of the gastrointestinal tract T-cell lymphoma Pollakisuria B lymphocytopenia Decrease in T cell count Abnormal hair quantity Rhabdomyosarcoma Glioma Medulloblastoma Recurrent sinopulmonary infections Skeletal dysplasia Rigidity Acute leukemia Recurrent otitis media Sleep apnea Acanthosis nigricans Paraparesis Clonus Short toe Rhizomelia Abnormal lung morphology Abnormality of the metaphysis Abnormal form of the vertebral bodies Osteoarthritis Conductive hearing impairment Epidermal acanthosis Lumbar hyperlordosis Overgrowth Sleep disturbance Confusion Micromelia Joint hyperflexibility Scarring Hyperlordosis Apnea Recurrent bronchitis Acute lymphoblastic leukemia Central diabetes insipidus Abnormality of the inner ear Respiratory insufficiency Short neck Skeletal muscle atrophy Muscle weakness Absence of Stensen duct Generalized microdontia Periorbital hyperpigmentation Transverse vaginal septum Mesoaxial polydactyly Aplasia/Hypoplasia of the breasts Macrotia Megacystis Urethral atresia Dacryocystitis Ureterocele Abnormality of the middle ear Nail pits Abnormality of the nasopharynx Thin nail Urethral stenosis Selective tooth agenesis Hyperactivity Retrognathia Anal stenosis Abnormality of the hair Abnormality of the musculature Freckling Long nose Non-midline cleft lip Abnormality of neuronal migration Premature ovarian insufficiency Deep philtrum Cachexia Recurrent pneumonia Low anterior hairline Abnormality of the face Intellectual disability, moderate Primary amenorrhea Cutaneous photosensitivity Amenorrhea Convex nasal ridge Prominent nose Neurodegeneration Hemolytic anemia Prominent nasal bridge Attention deficit hyperactivity disorder Mental deterioration Decreased T cell activation


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