Lymphoma, and Insulin resistance

Diseases related with Lymphoma and Insulin resistance

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


Top matches:

Medium match FOLLICULAR LYMPHOMA


Follicular lymphoma is a form of non-Hodgkin lymphoma (see this term) characterized by a proliferation of B cells whose nodular structure of follicular architecture is preserved.

FOLLICULAR LYMPHOMA Is also known as oncogene b-cell leukemia 2

Related symptoms:

  • Neoplasm
  • Fever
  • Fatigue
  • Diarrhea
  • Splenomegaly


SOURCES: OMIM ORPHANET MENDELIAN

More info about FOLLICULAR LYMPHOMA

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

Low match WERNER SYNDROME


Werner syndrome (WS) is a rare inherited syndrome characterized by premature aging with onset in the third decade of life and with cardinal clinical features including bilateral cataracts, short stature, graying and thinning of scalp hair, characteristic skin disorders and premature onset of additional age-related disorders.

WERNER SYNDROME Is also known as ws|adult progeria

Related symptoms:

  • Short stature
  • Neoplasm
  • Pain
  • Cataract
  • Visual impairment


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about WERNER SYNDROME

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Other less relevant matches:

Low match LIG4 SYNDROME


LIG4 syndrome is a hereditary disorder associated with impaired DNA double-strand break repair mechanisms and characterized by microcephaly, unusual facial features, growth and developmental delay, skin anomalies, and pancytopenia, which is associated with combined immunodeficiency (CID).

LIG4 SYNDROME Is also known as dna ligase iv deficiency|ligase 4 syndrome

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Microcephaly
  • Growth delay
  • Micrognathia


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about LIG4 SYNDROME

Low match PRADER-WILLI SYNDROME; PWS


Prader-Willi syndrome is characterized by diminished fetal activity, obesity, muscular hypotonia, mental retardation, short stature, hypogonadotropic hypogonadism, and small hands and feet. It can be considered to be an autosomal dominant disorder and is caused by deletion or disruption of a gene or several genes on the proximal long arm of the paternal chromosome 15 or maternal uniparental disomy 15, because the gene(s) on the maternal chromosome(s) 15 are virtually inactive through imprinting. Horsthemke and Wagstaff (2008) provided a detailed review of the mechanisms of imprinting of the Prader-Willi/Angelman syndrome (OMIM ) region.See also the chromosome 15q11-q13 duplication syndrome (OMIM ), which shows overlapping clinical features.

PRADER-WILLI SYNDROME; PWS Is also known as prader-labhart-willi syndrome

Related symptoms:

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


SOURCES: OMIM MENDELIAN

More info about PRADER-WILLI SYNDROME; PWS

Low match CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1


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

Low match COMBINED IMMUNODEFICIENCY DUE TO LRBA DEFICIENCY


Common variable immunodeficiency-8 with autoimmunity is an autosomal recessive disorder of immune dysregulation. Affected individuals have early childhood onset of recurrent infections, particularly respiratory infections, and also develop variable autoimmune disorders, including idiopathic thrombocytopenic purpura, autoimmune hemolytic anemia, and inflammatory bowel disease. The presentation and phenotype are highly variable, even within families (summary by Lopez-Herrera et al., 2012 and Alangari et al., 2012). Immunologic findings are also variable and may include decreased B cells, hypogammaglobulinemia, and deficiency of CD4+ T regulatory (Treg) cells (Charbonnier et al., 2015).For a general description and a discussion of genetic heterogeneity of common variable immunodeficiency, see CVID1 (OMIM ).

COMBINED IMMUNODEFICIENCY DUE TO LRBA DEFICIENCY Is also known as cid due to lrba deficiency

Related symptoms:

  • Growth delay
  • Neoplasm
  • Failure to thrive
  • Anemia
  • Diarrhea


SOURCES: OMIM ORPHANET MENDELIAN

More info about COMBINED IMMUNODEFICIENCY DUE TO LRBA DEFICIENCY

Low match BLOOM SYNDROME


Bloom syndrome (BSyn) is a rare chromosomal breakage syndrome characterized by a marked genetic instability associated with pre- and postnatal growth retardation, facial sun-sensitive telangiectatic erythema, increased susceptibility to infections, and predisposition to cancer.

BLOOM SYNDROME Is also known as bls|microcephaly, growth restriction, and increased sister chromatid exchange 1|bs|bsyn|mgrisce1

Related symptoms:

  • Short stature
  • Microcephaly
  • Growth delay
  • Neoplasm
  • Failure to thrive


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about BLOOM SYNDROME

Low match BANNAYAN-RILEY-RUVALCABA SYNDROME


Bannayan-Riley-Ruvalcaba syndrome (BRRS) is a rare congenital disorder characterized by hamartomatous intestinal polyposis, lipomas, macrocephaly and genital lentiginosis.

BANNAYAN-RILEY-RUVALCABA SYNDROME Is also known as brrs|myhre-riley-smith syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Scoliosis


SOURCES: ORPHANET MENDELIAN

More info about BANNAYAN-RILEY-RUVALCABA SYNDROME

Top 5 symptoms//phenotypes associated to Lymphoma and Insulin resistance

Symptoms // Phenotype % cases
Neoplasm Common - Between 50% and 80% cases
Leukemia Common - Between 50% and 80% cases
Short stature Common - Between 50% and 80% cases
Diabetes mellitus Uncommon - Between 30% and 50% cases
Micrognathia Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Failure to thrive Growth delay Myeloid leukemia Anemia Cryptorchidism Dolichocephaly Telangiectasia Type I diabetes mellitus Global developmental delay Intellectual disability Type II diabetes mellitus Weight loss Diarrhea Congestive heart failure Chromosome breakage Recurrent respiratory infections Thrombocytopenia Clinodactyly of the 5th finger Hypogonadism IgA deficiency Upslanted palpebral fissure Abnormality of the dentition Infertility Hypothyroidism Postnatal growth retardation Abnormality of chromosome stability Short nose Spontaneous abortion Hypopigmentation of the skin Osteoporosis Seizures Cutaneous photosensitivity Recurrent infections Myelodysplasia Squamous cell carcinoma Fever Telangiectasia of the skin Intrauterine growth retardation Pancytopenia Immunodeficiency Epicanthus Scoliosis Respiratory tract infection Fatigue Glucose intolerance Lymphadenopathy Neutropenia Microcephaly

Rare Symptoms - Less than 30% cases


Erythema Malabsorption Hypopigmented skin patches Pain Azoospermia Nevus Hypertension Polyphagia Hypergonadotropic hypogonadism Skeletal muscle atrophy Combined immunodeficiency Cafe-au-lait spot Ataxia Acute leukemia Alopecia High pitched voice Hyperinsulinemia Lymphedema Abnormality of the nervous system Cor pulmonale Meningioma Chronic lung disease Thyroid carcinoma Bronchiectasis IgM deficiency Abnormality of the testis Otitis media Decreased antibody level in blood Arteriovenous malformation Micropenis Almond-shaped palpebral fissure Inflammation of the large intestine Delayed skeletal maturation Irregular hyperpigmentation Pneumonia Acute myeloid leukemia Multiple cafe-au-lait spots Delayed speech and language development Oligohydramnios Behavioral abnormality Muscular hypotonia Splenomegaly Syndactyly Hypoglycemia Hepatomegaly Narrow face Carcinoma B-cell lymphoma Abnormal intestine morphology Chronic diarrhea Inflammatory abnormality of the skin Proptosis Cataract High palate Autoimmunity Severe short stature Respiratory failure Irritability Visual impairment Abnormal facial shape Specific learning disability Intellectual disability, mild Finger syndactyly Vomiting Strabismus Myopathy Delayed puberty Small hand Abnormality of the skeletal system Nystagmus Ventriculomegaly Frontal bossing Acrocyanosis Poor fine motor coordination Polyneuropathy Abdominal obesity Hypoplasia of the fovea Hypothermia Ocular albinism Abdominal distention Generalized hypopigmentation Erysipelas Anteverted ears Abdominal pain Narrow palm Psychotic episodes Overweight Poor gross motor coordination Acromicria Hypoplastic labia minora Depressivity Central adrenal insufficiency Clitoral hypoplasia Arthralgia Temperature instability Elevated hepatic transaminase Triangular mouth Disseminated intravascular coagulation Hypopnea Frontal upsweep of hair Anxiety Oligomenorrhea Hyperreflexia Central hypotonia Esotropia Clumsiness Primary amenorrhea Psychosis Decreased fetal movement Narrow forehead Abnormality of the cardiovascular system Amenorrhea Hip dysplasia Febrile seizures Growth hormone deficiency Gastrointestinal hemorrhage Aortic valve stenosis Full cheeks Sepsis Sleep disturbance Tapered finger Short foot Downturned corners of mouth Short palm Polymicrogyria Arachnodactyly Genu valgum Carious teeth Bradycardia Increased body weight Abnormality of lipid metabolism Skeletal muscle hypertrophy Iris hypopigmentation Hypoventilation Hypopigmentation of hair Pulmonary embolism Striae distensae Impaired pain sensation Narrow nasal bridge External genital hypoplasia Truncal obesity Decreased muscle mass Adrenal insufficiency Albinism Hypogonadotrophic hypogonadism Large hands Emotional lability Radial deviation of finger Failure to thrive in infancy Nasal speech Poor suck Infantile muscular hypotonia Scrotal hypoplasia Sleep apnea Bicuspid aortic valve Narrow palpebral fissure Precocious puberty Prolonged partial thromboplastin time Cerebral calcification Abnormality of the nose Long philtrum Anteverted nares Macrocephaly Muscle weakness Facial telangiectasia in butterfly midface distribution Agenesis of maxillary lateral incisor Neoplasm of the gastrointestinal tract Spotty hyperpigmentation Spotty hypopigmentation Female infertility Decreased fertility in females Chronic obstructive pulmonary disease Macrotia Hypoplastic pelvis Hypoplasia of the zygomatic bone IgG deficiency Hodgkin lymphoma Pulmonary fibrosis Hand polydactyly Reduced number of teeth Sacral dimple Sinusitis Abnormality of the face Hypertrichosis Pectus excavatum Neurological speech impairment Prominent nose Lipoma Abnormal large intestine morphology Uterine neoplasm Abdominal wall muscle weakness Subcutaneous hemorrhage Hamartomatous polyposis Neoplasm of the breast Visceral angiomatosis Intestinal polyposis Angina pectoris Abnormality of the optic nerve Capillary hemangioma Hashimoto thyroiditis Joint hyperflexibility Hamartoma Multiple lipomas Cutis marmorata Aortic aneurysm Intracranial hemorrhage Cachexia Delayed gross motor development Narrow palate Tall stature Subcutaneous nodule Broad thumb Wide nose Abnormality of the skin Ichthyosis Eczema Pruritus Hemolytic anemia Arthritis Hepatosplenomegaly Vitamin B12 deficiency Vitamin K deficiency Vitamin D deficiency Folate deficiency Abnormality of the abdominal wall Prolonged prothrombin time Recurrent aphthous stomatitis Stomatitis Chronic fatigue Recurrent otitis media Thrombocytosis Iron deficiency anemia Thyroiditis Macrocytic anemia Celiac disease Steatorrhea Malnutrition Abnormality of the coagulation cascade Rickets Hypocalcemia Hypoplasia of dental enamel Asthma Abnormal lung morphology Skin rash Verrucae Protruding ear Polydactyly Hyperhidrosis Malar flattening Cardiomyopathy Burkitt lymphoma Follicular hyperplasia Generalized lymphadenopathy Interstitial pneumonitis Gastritis Immune dysregulation Brain neoplasm Conjunctivitis Villous atrophy Clubbing of fingers Exocrine pancreatic insufficiency Autoimmune thrombocytopenia Fatigable weakness Recurrent sinusitis Autoimmune hemolytic anemia Colitis Interstitial pulmonary abnormality Clubbing Recurrent upper respiratory tract infections Purpura Hypermetropia Feeding difficulties Stroke Abnormality of the uterus Reticulocytopenia Skin nodule Abnormal localization of kidney Abnormal renal morphology Abnormal aortic valve morphology Abnormality of the hypothalamus-pituitary axis Acute monocytic leukemia Abnormality of femur morphology Bicornuate uterus Abnormality of the thumb Aplastic anemia Abnormality of nervous system morphology Abnormality of the upper limb Abnormality of the ulna Abnormal eyelid morphology Mediastinal lymphadenopathy Hearing abnormality External ear malformation Aplasia/Hypoplasia of the radius Absent radius Abnormality of blood and blood-forming tissues Abnormality of the peritoneum Absent thumb Abnormal aortic morphology Primary hypothyroidism Ectopic kidney Abnormal carotid artery morphology Night sweats Peripheral neuropathy Abnormality of the preputium Pyridoxine-responsive sideroblastic anemia Aplasia/Hypoplasia of fingers Aplasia/Hypoplasia of the uvula Neoplasm of head and neck Deficient excision of UV-induced pyrimidine dimers in DNA Anemic pallor Prolonged G2 phase of cell cycle Compensated hypothyroidism Duodenal stenosis Absent testis Hypoplastic anemia Chromosomal breakage induced by crosslinking agents Decreased fertility in males Clubbing of toes Partial duplication of thumb phalanx Complete duplication of thumb phalanx Aplasia/Hypoplasia of the iris Low-grade fever Meckel diverticulum Duplicated collecting system Hydroureter Hearing impairment Chronic lymphatic leukemia Umbilical hernia Abnormality of the foot Toe syndactyly Hip dislocation Small for gestational age Abnormal cardiac septum morphology Abnormality of the liver Abnormality of the kidney Abnormality of the eye Hypertrophic cardiomyopathy Pes planus Cleft palate Anal atresia Ptosis Abnormal heart morphology Patent ductus arteriosus Hypospadias Abnormality of cardiovascular system morphology Headache Microphthalmia Renal insufficiency Atrial septal defect Hydrocephalus Respiratory distress Facial asymmetry Astigmatism Hypoplasia of the ulna Abnormal vertebral morphology Tracheoesophageal fistula Triphalangeal thumb Abnormality of the urinary system Abnormality of vision Reduced bone mineral density Renal hypoplasia/aplasia Cranial nerve paralysis Leukopenia Horseshoe kidney Bone marrow hypocellularity Spina bifida Short thumb Vertigo Recurrent urinary tract infections Aganglionic megacolon Abnormality of the genital system Choanal atresia Short palpebral fissure Hypertelorism Sloping forehead Tetralogy of Fallot Renal agenesis Bruising susceptibility Abnormality of skin pigmentation Rod-cone dystrophy Hyperkeratosis Attention deficit hyperactivity disorder Acral lentiginous melanoma Biparietal narrowing Leukocytosis Psoriasiform dermatitis Low anterior hairline Hypoplasia of penis Thin vermilion border Telecanthus Brachycephaly Meningitis Wide nasal bridge Aplasia/Hypoplasia of the testes Abnormality of bone marrow cell morphology Neoplasm of the oral cavity Premature arteriosclerosis Gastrointestinal carcinoma Neoplasm of the small intestine Subcutaneous calcification Poliosis Abnormal hair whorl Soft tissue sarcoma Chorioretinitis Cutaneous melanoma Narrow nasal ridge Severe combined immunodeficiency Bird-like facies Enlarged joints Clinodactyly Abnormality of the pinna Apnea Neonatal hypotonia Photophobia Thin upper lip vermilion Osteopenia Narrow mouth Autism Hyperactivity Prominent forehead Hyporeflexia Obesity Large beaked nose Dilatation Kyphosis Intellectual disability, severe Edema Talipes equinovarus Myopia Depressed nasal bridge Motor delay Cognitive impairment Generalized hypotonia Nausea Arteriosclerosis White forelock Joint stiffness Abnormality of the hair Lipodystrophy Dermal atrophy Sarcoma Laryngomalacia Breast carcinoma Melanoma Atherosclerosis Macular degeneration Hoarse voice Increased bone mineral density Skin ulcer Polydipsia Abnormality of retinal pigmentation Decreased body weight Sparse scalp hair Myocardial infarction Decreased testicular size Convex nasal ridge Chest pain Coma Nephropathy Retinal degeneration Retinopathy Abnormality of the voice Abnormality of the thorax Slender build Alopecia of scalp Pili torti Chondrocalcinosis Lack of skin elasticity Peripheral arterial stenosis Abnormality of the cerebral vasculature Osteosarcoma Renal neoplasm Progeroid facial appearance Posterior subcapsular cataract Pulmonary artery stenosis Neoplasm of the lung Premature loss of teeth Rocker bottom foot Subcapsular cataract Prematurely aged appearance Ovarian neoplasm Secondary amenorrhea Scleroderma Pleural effusion Aplasia/Hypoplasia of the skin Lipoatrophy Decreased fertility Premature graying of hair Polyuria Neoplasm of the adrenal cortex



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Intrauterine growth retardation and Sparse scalp hair, related diseases and genetic alterations Macrocephaly and Facial asymmetry, related diseases and genetic alterations

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