Lymphoma, and Squamous cell carcinoma

Diseases related with Lymphoma and Squamous cell carcinoma

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


Top matches:

Medium match NTHL1-RELATED ATTENUATED FAMILIAL ADENOMATOUS POLYPOSIS


Familial adenomatous polyposis-3 is an autosomal recessive cancer predisposition syndrome characterized by the development of multiple colonic adenomas, often with progression to colorectal cancer. Carcinomas affecting other tissues may also occur, and the carcinomas tend to develop in middle age or late adulthood (summary by Weren et al., 2015).For a discussion of genetic heterogeneity of familial adenomatous polyposis, see FAP1 (OMIM ).

NTHL1-RELATED ATTENUATED FAMILIAL ADENOMATOUS POLYPOSIS Is also known as nthl1-related attenuated fap|nthl1-related afap

Related symptoms:

  • Neoplasm
  • Carcinoma
  • Nevus
  • Lymphoma
  • Neoplasm of the skin


SOURCES: OMIM ORPHANET MENDELIAN

More info about NTHL1-RELATED ATTENUATED FAMILIAL ADENOMATOUS POLYPOSIS

Medium match THYROID CARCINOMA, FAMILIAL MEDULLARY; MTC


Medullary thyroid carcinoma (MTC) is a malignant tumor of the calcitonin (OMIM )-secreting parafollicular C cells of the thyroid, and occurs sporadically or as a component of the multiple endocrine neoplasia (MEN) type 2 (see {171400})/familial medullary thyroid carcinoma (FMTC) syndromes (summary by Abu-Amero et al., 2006). Thyroid cancer derived from follicular epithelial cells is referred to as nonmedullary thyroid cancer and comprises several subtypes; see {188550}.

THYROID CARCINOMA, FAMILIAL MEDULLARY; MTC Is also known as mtc1|fmtc

Related symptoms:

  • Neoplasm
  • Pain
  • Respiratory distress
  • Hypothyroidism
  • Carcinoma


SOURCES: OMIM MENDELIAN

More info about THYROID CARCINOMA, FAMILIAL MEDULLARY; MTC

Medium match IDIOPATHIC CD4 LYMPHOCYTOPENIA


Idiopathic CD4 lymphocytopenia is a rare primary immunodeficiency disorder characterized by persistent CD4 T-cell lymphopenia (less than 300 cells/µL on multiple occasions) not associated with any other underlying primary or secondary immune deficiency. Patients typically present opportunistic infections (with cryptococcal, mycobacterial, candidal, varicella zoster virus infections and progressive multifocal leukoencephalopathy being the most prevalent), malignancies (mainly lymphoproliferative disorders), or autoimmune disorders. Some individuals are asymptomatic and incidentally diagnosed.

IDIOPATHIC CD4 LYMPHOCYTOPENIA Is also known as icl|idiopathic cd4 lymphopenia

Related symptoms:

  • Neoplasm
  • Anemia
  • Immunodeficiency
  • Pneumonia
  • Carcinoma


SOURCES: OMIM ORPHANET MENDELIAN

More info about IDIOPATHIC CD4 LYMPHOCYTOPENIA

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Other less relevant matches:

Medium match PUNCTATE PALMOPLANTAR KERATODERMA TYPE 1


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

Medium match HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT


Hyper-IgE recurrent infection syndrome is a primary immunodeficiency disorder characterized by chronic eczema, recurrent Staphylococcal infections, increased serum IgE, and eosinophilia. Patients have a distinctive coarse facial appearance, abnormal dentition, hyperextensibility of the joints, and bone fractures (Buckley et al., 1972; Grimbacher et al., 1999).

HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT Is also known as hies, autosomal dominant|hyper-ige syndrome, autosomal dominant|job syndrome

Related symptoms:

  • Scoliosis
  • Hypertelorism
  • Strabismus
  • High palate
  • Wide nasal bridge


SOURCES: OMIM MENDELIAN

More info about HYPER-IGE RECURRENT INFECTION SYNDROME, AUTOSOMAL DOMINANT

Medium 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

Medium match DYSKERATOSIS CONGENITA


Dyskeratosis congenita (DC) is a rare ectodermal dysplasia that often presents with the classic triad of nail dysplasia, skin pigmentary changes, and oral leukoplakia associated with a high risk of bone marrow failure (BMF) and cancer.

DYSKERATOSIS CONGENITA Is also known as dkc|dc|dyskeratosis congenita, scoggins type|zinsser-engman-cole syndrome

Related symptoms:

  • Global developmental delay
  • Short stature
  • Hearing impairment
  • Microcephaly
  • Scoliosis


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about DYSKERATOSIS CONGENITA

Medium match HOYERAAL-HREIDARSSON SYNDROME


Hoyeraal-Hreidarsson syndrome (HHS) is a very rare X-linked recessive disorder considered to be a severe variant of dyskeratosis congenita (see this term) characterized by intrauterine growth retardation, microcephaly, cerebellar hypoplasia, progressive combined immune deficiency and aplastic anemia.

HOYERAAL-HREIDARSSON SYNDROME Is also known as progressive pancytopenia-immunodeficiency-cerebellar hypoplasia syndrome|zinsser-cole-engman syndrome

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about HOYERAAL-HREIDARSSON SYNDROME

Medium match CARTILAGE-HAIR HYPOPLASIA


Cartilage-hair hypoplasia is a disease affecting the bone metaphyses causing small stature from birth.

CARTILAGE-HAIR HYPOPLASIA Is also known as autosomal recessive metaphyseal chondrodysplasia|metaphyseal chondrodysplasia, mckusick type

Related symptoms:

  • Intellectual disability
  • Short stature
  • Scoliosis
  • Growth delay
  • Neoplasm


SOURCES: OMIM ORPHANET MENDELIAN

More info about CARTILAGE-HAIR HYPOPLASIA

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

Top 5 symptoms//phenotypes associated to Lymphoma and Squamous cell carcinoma

Symptoms // Phenotype % cases
Neoplasm Very Common - Between 80% and 100% cases
Carcinoma Common - Between 50% and 80% cases
Hodgkin lymphoma Common - Between 50% and 80% cases
Immunodeficiency Common - Between 50% and 80% cases
Anemia Common - Between 50% and 80% cases
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Other less frequent symptoms

Patients with Lymphoma and Squamous cell carcinoma. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Short stature Growth delay Leukemia Scoliosis Abnormality of the dentition Microcephaly Failure to thrive Intrauterine growth retardation Pneumonia Strabismus Thrombocytopenia Aplastic anemia Cataract Pancytopenia Abnormality of the skeletal system Hypopigmentation of the skin Recurrent infections Osteoporosis Visual impairment Intellectual disability Myelodysplasia Cryptorchidism Bone marrow hypocellularity Severe short stature Alopecia Abnormality of skin pigmentation Ataxia Hyperhidrosis Diabetes mellitus Postnatal growth retardation Hypopigmented skin patches Pulmonary fibrosis Myeloid leukemia Hepatomegaly Chromosome breakage Abnormality of chromosome stability Global developmental delay Hearing impairment Acute myeloid leukemia Telangiectasia Sinusitis Otitis media Neoplasm of the pancreas Neoplasm of the skin Lymphopenia Aganglionic megacolon Respiratory distress

Rare Symptoms - Less than 30% cases


B-cell lymphoma Finger syndactyly Dolichocephaly Specific learning disability Decreased antibody level in blood Recurrent respiratory infections Urethral stenosis Testicular atrophy Bronchiectasis Reticular hyperpigmentation Basal cell carcinoma Clinodactyly of the 5th finger Delayed skeletal maturation Cafe-au-lait spot Diarrhea Cardiomyopathy Inflammatory abnormality of the skin Micrognathia Breast carcinoma Ventriculomegaly Hypospadias Small for gestational age Abnormal cardiac septum morphology Sacral dimple Cellular immunodeficiency Dermal atrophy Hyperpigmentation of the skin Cirrhosis Malabsorption Carious teeth Nail dystrophy Sparse hair Cerebellar hypoplasia Pain Splenomegaly Hypothyroidism Abnormal intestine morphology Tracheoesophageal fistula Azoospermia Epiphora Premature graying of hair Abnormality of coagulation Dilatation Hypoplastic anemia Premature loss of teeth Blepharitis Telangiectasia of the skin Abnormality of the testis Oral leukoplakia Ridged nail Oligohydramnios Gastrointestinal hemorrhage Cerebral calcification Skin ulcer Sparse eyelashes Frontal bossing Joint hypermobility Recurrent fractures Epicanthus Facial asymmetry Neutropenia High palate Prominent nose Leukopenia Wide nasal bridge Hypertelorism Opportunistic infection Skin rash Bronchiolitis Abnormality of the skin Palmoplantar keratoderma Recurrent sinusitis Constipation Hyperkeratosis Horseshoe kidney Erythema Prominent forehead Spinal dysraphism Mucopolysacchariduria Large face Blue sclerae Hypersplenism Normocytic anemia Abnormal diaphysis morphology Fine hair Congenital hypoplastic anemia Mesomelia Neonatal short-limb short stature Short palm Neoplasm of head and neck Arthrogryposis multiplex congenita Abnormality of the distal phalanx of finger Hypotrichosis Narrow chest Joint hyperflexibility Aplasia/Hypoplasia of the uvula Micromelia Small hand Abnormal bone ossification Abnormal T cell morphology Postural instability Convex nasal ridge Aplasia/Hypoplasia of fingers Abnormality of the ribs Depressed nasal ridge Lumbar hyperlordosis Abnormally ossified vertebrae Diaphyseal thickening Rhizomelia Abnormality of the metaphysis Hypoplasia of the odontoid process Abnormality of pelvic girdle bone morphology Genu varum Narrow vertebral interpedicular distance Portal hypertension Exocrine pancreatic insufficiency Distal arthrogryposis Metaphyseal widening Esophageal atresia Anal stenosis Reduced tendon reflexes Macrocytic anemia Metaphyseal dysplasia High hypermetropia Cone-shaped epiphysis Pyridoxine-responsive sideroblastic anemia Abnormality of the hip bone Tibial bowing Limited elbow extension Short thorax Disproportionate short-limb short stature Abnormal palate morphology Abnormal form of the vertebral bodies Abnormality of the pancreas Bowing of the long bones Abnormality of epiphysis morphology Femoral bowing Metaphyseal cupping Metaphyseal chondrodysplasia Abnormality of retinal pigmentation Gingival overgrowth Aplasia/Hypoplasia affecting the eye Aplasia/Hypoplasia of the abdominal wall musculature Sparse and thin eyebrow Accelerated skeletal maturation Generalized joint laxity Tracheal stenosis Fair hair Heart block Short ribs Hypocalcemia Upper limb undergrowth Overweight Thrombocytosis Reticulocytopenia Susceptibility to chickenpox Long fibula Insulin resistance Triphalangeal thumb Hyperinsulinemia Abnormality of the urinary system Abnormality of vision Reduced bone mineral density Renal hypoplasia/aplasia Cranial nerve paralysis Type I diabetes mellitus Hypergonadotropic hypogonadism Spina bifida Abnormal vertebral morphology Short thumb Hypoplasia of the ulna Recurrent urinary tract infections Abnormality of the genital system Choanal atresia Short palpebral fissure Sloping forehead Tetralogy of Fallot Renal agenesis Bruising susceptibility Vertigo Astigmatism Anal atresia Glucose intolerance Ectopic kidney Toe syndactyly Abnormality of the ulna 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 Abnormality of the uterus Abnormality of the upper limb Arteriovenous malformation Abnormal aortic morphology Hydroureter Abnormal eyelid morphology Abnormality of nervous system morphology Primary hypothyroidism Hearing abnormality External ear malformation Irregular hyperpigmentation Aplasia/Hypoplasia of the radius Absent radius Abnormality of blood and blood-forming tissues Multiple cafe-au-lait spots Absent thumb Abnormality of the foot Hip dislocation Non-Hodgkin lymphoma Almond-shaped palpebral fissure Absent testis Hydrocephalus Fatigue Fever Hyperreflexia Compensated hypothyroidism Ptosis Cleft palate Abnormal facial shape Nystagmus Pulmonary lymphoma Flaring of lower rib cage Decreased fertility in males Absent pubertal growth spurt Abnormality of humoral immunity Biconvex vertebral bodies Severe T-cell immunodeficiency Sparse facial hair Abnormal carotid artery morphology Prolonged G2 phase of cell cycle Anemic pallor Deficient excision of UV-induced pyrimidine dimers in DNA Impaired lymphocyte transformation with phytohemagglutinin Metaphyseal dysostosis Chromosomal breakage induced by crosslinking agents Atrial septal defect Abnormality of the liver Proptosis Irritability Abnormality of the kidney Duodenal stenosis Duplicated collecting system Abnormality of the eye Hypertrophic cardiomyopathy Pes planus Umbilical hernia Meckel diverticulum Low-grade fever Aplasia/Hypoplasia of the iris Complete duplication of thumb phalanx Congestive heart failure Weight loss Partial duplication of thumb phalanx Upslanted palpebral fissure Hypogonadism Abnormal heart morphology Patent ductus arteriosus Abnormality of cardiovascular system morphology Headache Microphthalmia Clubbing of toes Renal insufficiency Pectus carinatum Absent lacrimal punctum Hyperlordosis Hemihypertrophy Recurrent fungal infections Fractures of the long bones B lymphocytopenia Persistence of primary teeth Decrease in T cell count Red hair Increased IgE level Recurrent sinopulmonary infections Verrucae Chronic mucocutaneous candidiasis Eczematoid dermatitis Recurrent bronchitis Atopic dermatitis Bronchitis Chronic otitis media Urticaria Recurrent skin infections Eosinophilia Recurrent bacterial infections Hemivertebrae T-cell lymphoma Recurrent bacterial skin infections Eczema Polydactyly Reduced number of teeth Narrow face Abnormality of the face Hypertrichosis Cutaneous photosensitivity Type II diabetes mellitus Ichthyosis Infertility Protruding ear Syndactyly Onychomycosis Malar flattening Short nose Intellectual disability, mild Impaired neutrophil chemotaxis Squamous cell carcinoma of the vulva Anal canal squamous carcinoma Lung abscess Recurrent candida infections Recurrent Staphylococcus aureus infections Severe viral infections Thick lower lip vermilion Asthma High pitched voice Thyroiditis Recurrent otitis media Hemolytic anemia Cutaneous amyloidosis Follicular thyroid carcinoma Medullary thyroid carcinoma Papillary thyroid carcinoma Teratoma Thyroid carcinoma Neoplasm of the endocrine system Amyloidosis Autoimmune hemolytic anemia Goiter Hoarse voice Lymphadenopathy Duodenal adenocarcinoma Bladder carcinoma Bladder neoplasm Prostate cancer Meningioma Nevus Psoriasiform dermatitis Papilloma Wide nose Orthokeratosis Pruritus Cough Craniosynostosis Deeply set eye Coarse facial features Osteopenia Mandibular prognathia Dysphagia Transitional cell carcinoma of the bladder Hypergranulosis Bronchiolitis obliterans Parakeratosis Renal cell carcinoma Colon cancer Scaling skin Abnormality of the nail Thickened skin Epidermal acanthosis Papule Depressivity Bronchiolitis obliterans organizing pneumonia Hand polydactyly IgA deficiency Low-set, posteriorly rotated ears Conjunctivitis Esophageal stricture Excessive wrinkled skin Generalized hyperpigmentation Restrictive ventilatory defect Increased antibody level in blood Flared metaphysis Neonatal respiratory distress Pterygium Anosmia Truncal ataxia Lacrimal duct stenosis Sparse scalp hair Decreased fetal movement Decreased testicular size Gliosis Sepsis Muscular hypotonia of the trunk Hepatosplenomegaly Cerebral cortical atrophy Hyporeflexia Keratoconjunctivitis Pancreatic adenocarcinoma Optic atrophy Hypertension Joint laxity EEG abnormality Skeletal dysplasia Macrotia Brachycephaly Short neck Respiratory insufficiency Anteverted nares Myopia Depressed nasal bridge Abnormal leukocyte morphology Cognitive impairment Muscular hypotonia Anal mucosal leukoplakia Pterygium of nails Split nail Generalized hypopigmentation of hair Fragile teeth Brittle scalp hair Reticulated skin pigmentation Phimosis Hypertonia Generalized hypotonia IgG deficiency Neoplasm of the gastrointestinal tract Abnormality of the fingernails Hepatic fibrosis Abnormal blistering of the skin Nail dysplasia Hypoplasia of the maxilla Hypodontia Hepatic failure Facial telangiectasia in butterfly midface distribution Agenesis of maxillary lateral incisor Spotty hyperpigmentation Neurofibromas Spotty hypopigmentation Female infertility Decreased fertility in females IgM deficiency Abnormality of the nose Chronic obstructive pulmonary disease Chronic lung disease Hypoplastic pelvis Hypoplasia of the zygomatic bone Acute leukemia Hypermelanotic macule Macule Seizures Interstitial pneumonitis Esophageal stenosis Palmar hyperkeratosis Displacement of the external urethral meatus Congenital bullous ichthyosiform erythroderma Anorectal anomaly Nail pits Rough bone trabeculation Porokeratosis Aplastic/hypoplastic toenail Abnormality of neutrophils Skin vesicle Squamous cell carcinoma of the skin Abnormality of the pharynx Abnormality of female internal genitalia White hair Periodontitis Taurodontia Abnormal eyebrow morphology Abnormal eyelash morphology Aseptic necrosis Aplasia/Hypoplasia of the skin Abnormality of the preputium



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