Lymphoma, and Umbilical hernia

Diseases related with Lymphoma and Umbilical hernia

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

Top matches:

PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY; FPDMM Is also known as platelet disorder, aspirin-like|thrombocytopenia, familial, with propensity to acute myelogenous leukemia|fpd/aml

Related symptoms:

  • Anemia
  • Thrombocytopenia
  • Hernia
  • Hypospadias
  • Umbilical hernia


SOURCES: OMIM MENDELIAN

More info about PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY; FPDMM

Related symptoms:

  • Scoliosis
  • Neoplasm
  • Fever
  • Inguinal hernia
  • Arthralgia


SOURCES: OMIM MENDELIAN

More info about EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2; EDSPD2

Medium match WEAVER SYNDROME; WVS

Weaver syndrome comprises pre- and postnatal overgrowth, accelerated osseous maturation, characteristic craniofacial appearance, and developmental delay. Most cases are sporadic, although autosomal dominant inheritance has been reported. Although there is phenotypic overlap between Weaver syndrome and Sotos syndrome (OMIM ), distinguishing features of Weaver syndrome include broad forehead and face, ocular hypertelorism, prominent wide philtrum, micrognathia, deep horizontal chin groove, and deep-set nails. In addition, carpal bone development is advanced over the rest of the hand in Weaver syndrome, whereas in Sotos syndrome carpal bone development is at or behind that of the rest of the hand (summary by Basel-Vanagaite, 2010).The 'Weaver-like' syndrome reported by Stoll et al. (1985) in a mother and son may be a separate entity.Sotos syndrome (OMIM ), which shows considerable phenotypic overlap with Weaver syndrome, is caused by mutation in the NSD1 gene (OMIM ) on chromosome 5q35.

WEAVER SYNDROME; WVS Is also known as weaver-smith syndrome|wss

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Scoliosis


SOURCES: OMIM MENDELIAN

More info about WEAVER SYNDROME; WVS

Other less relevant matches:

Medium 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

Cardiofaciocutaneous (CFC) syndrome is a RASopathy characterized by craniofacial dysmorphology, congenital heart disease, dermatological abnormalities (most commonly hyperkeratotic skin and sparse, curly hair), growth retardation and intellectual disability.

CARDIOFACIOCUTANEOUS SYNDROME Is also known as cfcs|cfc syndrome

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about CARDIOFACIOCUTANEOUS SYNDROME

Autosomal dominant anomaly characterized by abnormal ovoid shape GRANULOCYTE nuclei and their clumping chromatin. Mutations in the LAMIN B receptor gene that results in reduced protein levels are associated with the disorder. Heterozygote individuals are healthy with normal granulocyte function while homozygote individuals occasionally have skeletal anomalies, developmental delay, and seizures.

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Hypertelorism
  • Failure to thrive
  • Strabismus


SOURCES: OMIM MESH MENDELIAN

More info about PELGER-HUET ANOMALY; PHA

Low match DOWN SYNDROME

Down syndrome is a chromosomal abnormality caused by the presence of a third (partial or total) copy of chromosome 21 and that is characterized by variable intellectual disability, muscular hypotonia, and joint laxity, often associated with a characteristic facial dysmorphism and various anomalies such as cardiac, gastrointestinal, or endocrine defects.

DOWN SYNDROME Is also known as trisomy 21

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Short stature
  • Generalized hypotonia
  • Hearing impairment


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about DOWN SYNDROME

Gaucher disease type 2 is the acute neurological form of Gaucher disease (GD; see this term). It is characterized by early-onset and severe neurological involvement of the brainstem, associated with an organomegaly and generally leading to death before the age of 2.

GAUCHER DISEASE TYPE 2 Is also known as infantile cerebral gaucher disease|acute neuronopathic gaucher disease

Related symptoms:

  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Microcephaly
  • Scoliosis


SOURCES: ORPHANET MENDELIAN

More info about GAUCHER DISEASE TYPE 2

Noonan syndrome-like disorder with juvenile myelomonocytic leukemia is a rare, genetic, polymalformative syndrome with increased risk of developing cancer characterized by a Noonan-like phenotype, including typical dysmorphic facial features (i.e. high forehead, hypertelorism, downslanting palpebral fissures, ptosis, low-set ears, prominent philtrum and short neck with or without pterygium colli), thoracic abnormalities, congenital heart defects and short stature, associated with a very frequent ocurrence of juvenile myelomonocytic leukemia. Developmental delay, ectodermal anomalies, joint laxity, and hypotonia may also be associated.

NOONAN SYNDROME-LIKE DISORDER WITH JUVENILE MYELOMONOCYTIC LEUKEMIA Is also known as cbl mutation-associated syndrome|noonan syndrome-like disorder with jmml|cbl syndrome

Related symptoms:

  • Global developmental delay
  • Short stature
  • Generalized hypotonia
  • Microcephaly
  • Growth delay


SOURCES: ORPHANET OMIM MENDELIAN

More info about NOONAN SYNDROME-LIKE DISORDER WITH JUVENILE MYELOMONOCYTIC LEUKEMIA

Baller-Gerold syndrome is characterized by the association of coronal craniosynostosis with radial ray anomalies (oligodactyly, aplasia or hypoplasia of the thumb, aplasia or hypoplasia of the radius).

BALLER-GEROLD SYNDROME Is also known as craniosynostosis-radial aplasia syndrome|craniosynostosis with radial defects

Related symptoms:

  • Intellectual disability
  • Seizures
  • Short stature
  • Hearing impairment
  • Scoliosis


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about BALLER-GEROLD SYNDROME

Top 5 symptoms//phenotypes associated to Lymphoma and Umbilical hernia

Symptoms // Phenotype % cases
Thrombocytopenia Common - Between 50% and 80% cases
Strabismus Common - Between 50% and 80% cases
Global developmental delay Common - Between 50% and 80% cases
Leukemia Common - Between 50% and 80% cases
Epicanthus Common - Between 50% and 80% cases

Other less frequent symptoms

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

Common Symptoms - More than 50% cases

Intellectual disability

Uncommon Symptoms - Between 30% and 50% cases

Scoliosis

Common Symptoms - More than 50% cases

Hypertelorism

Uncommon Symptoms - Between 30% and 50% cases

Abnormality of cardiovascular system morphology Short stature Anemia Generalized hypotonia Frontal bossing Failure to thrive Depressed nasal bridge Neoplasm Prominent forehead Edema Bruising susceptibility Hearing impairment Seizures Kyphosis Downslanted palpebral fissures Macrocephaly Neutropenia Growth delay Cryptorchidism Abnormal bleeding Muscular hypotonia Abnormal facial shape Micrognathia Hydrocephalus Abnormal heart morphology Irritability Acute lymphoblastic leukemia Inguinal hernia Ptosis Hydroureter Joint laxity Myopia Sparse hair Broad forehead Short nose Hydronephrosis Cafe-au-lait spot Optic atrophy Poor suck Cataract Nystagmus Fine hair Low-set, posteriorly rotated ears Feeding difficulties in infancy Lymphedema Proptosis Ventricular septal defect Gastroesophageal reflux Short neck Abnormality of the dentition Macrotia Splenomegaly Ataxia Microcephaly Polyhydramnios Behavioral abnormality High palate Respiratory distress Hernia Epistaxis Abnormality of the kidney Clinodactyly of the 5th finger Motor delay Acute monocytic leukemia Abnormal cardiac septum morphology Cholelithiasis Fever Failure to thrive in infancy Congestive heart failure Atrial septal defect Joint hypermobility Anal atresia Intrauterine growth retardation Bilateral ptosis Delayed skeletal maturation Long philtrum Astigmatism Hepatomegaly Pancytopenia Delayed speech and language development Hypertonia

Rare Symptoms - Less than 30% cases

Dolichocephaly Abnormality of blood and blood-forming tissues B-cell lymphoma Abnormality of the ulna Abnormality of skin pigmentation Hypertrophic cardiomyopathy Chromosome breakage Short thumb Aplasia/Hypoplasia of the radius Abnormality of the eye Absent radius Aganglionic megacolon Postnatal growth retardation Renal hypoplasia/aplasia Facial asymmetry Abnormal aortic valve morphology Multiple cafe-au-lait spots Absent thumb Abnormality of the foot Hypoplasia of the ulna Abnormal vertebral morphology Tracheoesophageal fistula Leukopenia Abnormality of vision Abnormality of the testis Pulmonic stenosis Abnormal localization of kidney Dementia Pleural effusion Ectropion Cubitus valgus Heart murmur Neurodevelopmental delay Short attention span Polydactyly Cognitive impairment Hypertension Gait disturbance Brachycephaly Narrow palate Narrow mouth Conductive hearing impairment Developmental regression Bilateral single transverse palmar creases Hypoxemia Hepatosplenomegaly Ascites Cyanosis Hydrops fetalis Abnormality of the thorax Abnormality of the spleen Deep philtrum Aspiration Duodenal stenosis High forehead Low-set ears Feeding difficulties Dysphagia Anteverted nares Cardiomyopathy Vomiting Malar flattening Pectus excavatum Encephalopathy Posteriorly rotated ears Osteopenia Hyperpigmentation of the skin Pectus carinatum Hypermetropia Hypotrichosis Falls Thick vermilion border Vesicoureteral reflux Webbed neck Low posterior hairline Open mouth Decreased body weight Thickened skin Hypothyroidism Oculomotor apraxia Myelodysplasia Acute myeloid leukemia Hypospadias Fatigue Hyperextensible skin Abnormality of the skeletal system Ventriculomegaly Large for gestational age Spasticity Cutis laxa Prominent fingertip pads Cleft palate Hypoplastic iliac wing Hyperhidrosis Pes cavus Flexion contracture Purpura Upslanted palpebral fissure Hydrocele testis Dysarthria Dyspnea Weight loss Rigidity Jaundice Neuroblastoma Hypoglycemia Elevated hepatic transaminase Apnea Abdominal pain Acute leukemia Myoclonus Recurrent respiratory infections Arrhythmia Dystonia Diarrhea Cough Acute megakaryocytic leukemia Left-to-right shunt Round ear Brushfield spots Transient myeloproliferative syndrome Crackles Atlantoaxial instability Neutrophilia Abnormality of the fontanelles or cranial sutures Pallor Nausea Corneal opacity Cholestasis Clubbing Hyponatremia Portal hypertension Intracranial hemorrhage Hyperammonemia Osteolysis Hyperbilirubinemia Knee flexion contracture Hypocalcemia Elbow flexion contracture Cardiac arrest Bone pain Progressive microcephaly Anorexia Progressive neurologic deterioration Lethargy Pulmonary arterial hypertension Decreased fetal movement Prolonged bleeding time Abnormality of the skin Brain atrophy Syncope Generalized myoclonic seizures Pulmonary hypoplasia Hepatic failure Cirrhosis Abnormality of the lymphatic system Lymphadenopathy Abnormality of eye movement Ophthalmoplegia Shallow acetabular fossae Pulmonary edema Myeloproliferative disorder Lower limb hypertonia Nephroblastoma Atrophic scars Fragile skin Obesity Recurrent infections Gingival bleeding Brachydactyly Premature loss of teeth Periodontitis Short 3rd metacarpal Hyposegmentation of neutrophil nuclei Folate deficiency Median cleft palate Giant platelets Ectopic calcification Microtia Recurrent otitis media Multiple plantar creases Oral aversion Gingival recession Skeletal dysplasia Generalized tonic-clonic seizures Eczema Gingival overgrowth Short 5th metacarpal Foot dorsiflexor weakness Mild short stature Lower limb hyperreflexia Upper limb undergrowth Short 4th metacarpal Abnormality of chromosome segregation Osteoarthritis Flat face Short middle phalanx of the 5th finger Protruding tongue Prematurely aged appearance Abnormality of immune system physiology Impaired pain sensation Congenital hypothyroidism Neurofibrillary tangles Polycythemia Thrombocytosis Broad palm Thickened nuchal skin fold Double outlet right ventricle Senile plaques Impaired platelet aggregation Athetosis Complete atrioventricular canal defect Transposition of the great arteries Atrioventricular canal defect Short palm Type II diabetes mellitus Postaxial polydactyly Downturned corners of mouth Single transverse palmar crease Postural instability Macroglossia Microdontia Thick lower lip vermilion Decreased fertility Depressed nasal ridge Arthralgia Sandal gap Breast carcinoma Refractory anemia Alzheimer disease Akinesia Hypokinesia Menorrhagia Hypotelorism Oligodactyly Short humerus Aplasia/Hypoplasia of the thumb Anteriorly placed anus Narrow nasal bridge Hallux valgus Trigonocephaly Hypoplasia of the radius Abnormality of the metacarpal bones Spina bifida occulta Narrow face Large fontanelles Renal dysplasia Bowing of the long bones Underdeveloped nasal alae Abnormality of the ureter Abnormality of the subarachnoid space Reduced factor IX activity Hypoplasia of olfactory tract Reduced factor XII activity Juvenile myelomonocytic leukemia Reduced prothrombin activity Reduced factor X activity Agenesis of corpus callosum Prominent nose Craniosynostosis Skin rash Prominent nasal bridge Malabsorption Polymicrogyria Bifid uvula Fibular hypoplasia Carpal synostosis Arteritis Brachyturricephaly Aphalangy of the hands Anomalous splenoportal venous system Midface capillary hemangioma Carpal bone aplasia Persistent cloaca Limited shoulder movement Perineal fistula Bicoronal synostosis Aplasia of metacarpal bones Bilateral radial aplasia Flat forehead Urogenital fistula Abnormality of the carpal bones Metopic synostosis Ulnar bowing Shallow orbits Bilateral conductive hearing impairment Coronal craniosynostosis Choanal stenosis Osteosarcoma Rectovaginal fistula Poikiloderma Rib fusion Sagittal craniosynostosis Aplasia/Hypoplasia of the patella Oxycephaly Anterior plagiocephaly Patellar hypoplasia Hand oligodactyly Limited elbow movement Lambdoidal craniosynostosis Abnormality of the mediastinum Pulmonary lymphangiectasia Opisthotonus Hypomagnesemia Eclabion Abnormal pattern of respiration Histiocytosis Generalized osteosclerosis Restrictive deficit on pulmonary function testing Avascular necrosis of the capital femoral epiphysis Abnormality of the larynx Multiple myeloma Congenital nonbullous ichthyosiform erythroderma Supranuclear gaze palsy Nonimmune hydrops fetalis Slow saccadic eye movements Trismus Bulbar signs Fetal akinesia sequence Axial dystonia Congenital ichthyosiform erythroderma Abnormality of coagulation Petechiae Interstitial pulmonary abnormality Multiple palmar creases Exertional dyspnea Bulbar palsy Poor eye contact Aspiration pneumonia Atrophy/Degeneration affecting the brainstem Protuberant abdomen Limb hypertonia Epileptic spasms Hepatocellular carcinoma Increased serum ferritin Hemophagocytosis Abducens palsy Monocytosis Overfolded helix Hip dysplasia Mitral regurgitation Aortic valve stenosis Vasculitis Torticollis Bicuspid aortic valve Proximal placement of thumb Esotropia Decreased muscle mass Abnormal eyebrow morphology Facial hypotonia Hypochromic microcytic anemia Chylothorax Broad toe Wide intermamillary distance Triangular face Subcutaneous hemorrhage Erlenmeyer flask deformity of the femurs Spontaneous hematomas Intestinal bleeding Giant cell hepatitis Laryngeal stridor Orthopnea CSF pleocytosis Decreased beta-glucocerebrosidase protein and activity Highly arched eyebrow Hematological neoplasm Abnormal platelet aggregation Cardiac valve calcification Slowed horizontal saccades EEG with temporal sharp waves Myopathy Eyelid fasciculation Hyperkeratosis pilaris Abnormality of the auditory canal Partial duplication of thumb phalanx 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 Abnormal carotid artery morphology Almond-shaped palpebral fissure Compensated hypothyroidism Absent testis Hypoplastic anemia Chromosomal breakage induced by crosslinking agents Decreased fertility in males Clubbing of toes Complete duplication of thumb phalanx Abnormality of the preputium Aplasia/Hypoplasia of the iris Low-grade fever Meckel diverticulum Duplicated collecting system Broad philtrum Primary hypothyroidism Abnormality of nervous system morphology Abnormal aortic morphology Reticulocytopenia Abnormality of chromosome stability Dimple chin Abnormal renal morphology Poor fine motor coordination Abnormality of the hypothalamus-pituitary axis Pyridoxine-responsive sideroblastic anemia Dilation of lateral ventricles Bicornuate uterus Constipation Coxa valga Telecanthus Aggressive behavior Accelerated skeletal maturation EEG abnormality Coarse facial features Slurred speech Back pain Large hands Autism Hyperkeratosis Cerebral cortical atrophy Radial deviation of finger Alopecia Flat occiput Broad face Intellectual disability, severe Large earlobe Diastasis recti Down-sloping shoulders Prolactin excess Inverted nipples Secondary amenorrhea Blindness Metatarsus adductus Absent septum pellucidum Limited elbow extension Bilateral talipes equinovarus Overlapping toe Cerebral atrophy Depressivity Abnormality of femur morphology Abnormality of the thumb Respiratory tract infection Tetralogy of Fallot Hypergonadotropic hypogonadism Spina bifida Flared humeral metaphysis Insulin resistance Dysharmonic bone age Telangiectasia Recurrent urinary tract infections Visual impairment Abnormality of the genital system Choanal atresia Short palpebral fissure Hyperreflexia Oligohydramnios Sloping forehead Renal agenesis Horseshoe kidney Small for gestational age Carcinoma Diabetes mellitus Hypogonadism Severe short stature Abnormality of the liver Patent ductus arteriosus Finger syndactyly Hypopigmentation of the skin Hip dislocation Headache Toe syndactyly Microphthalmia Renal insufficiency Vertigo Bone marrow hypocellularity Type I diabetes mellitus Calcaneovalgus deformity Myeloid leukemia Abnormality of the uterus Aplastic anemia Abnormality of the upper limb Thoracolumbar kyphosis Arteriovenous malformation Thin nail Abnormal eyelid morphology Teratoma Hearing abnormality External ear malformation Irregular hyperpigmentation Galactorrhea Short fourth metatarsal Vertebral wedging Horizontal eyebrow Abnormally low-pitched voice Abnormality of the urinary system Azoospermia Cranial nerve paralysis Limited knee extension Hypopigmented skin patches Reduced bone mineral density Flared femoral metaphysis Hyperinsulinemia Deep-set nails Triphalangeal thumb Lumbar kyphosis Glucose intolerance Sacrococcygeal teratoma Squamous cell carcinoma Ectopic kidney Pointed chin Erythema Inappropriate crying Atopic dermatitis Abnormality of the optic nerve Dystrophic fingernails Abnormal hair pattern Thick upper lip vermilion Woolly hair Pain Abnormality of the gastrointestinal tract Premature skin wrinkling Hypoplasia of the zygomatic bone Absent eyelashes Enlarged kidney Arnold-Chiari type I malformation Abnormal eyelash morphology Alopecia of scalp Poor appetite Abnormal myocardium morphology Underdeveloped supraorbital ridges Anal stenosis Submucous cleft hard palate Generalized hyperpigmentation Curly hair Biparietal narrowing Abnormal heart valve morphology Long palpebral fissure Abnormality of the sternum Infantile spasms Neurofibromas Aplasia/Hypoplasia of the eyebrow Malnutrition Open bite Delayed CNS myelination Abnormality of refraction Obsessive-compulsive behavior Abnormality of the optic disc Cutaneous T-cell lymphoma Morphological abnormality of the gastrointestinal tract Puberty and gonadal disorders Abnormal location of ears Abnormality of the hairline Pes planus Tongue thrusting Functional abnormality of the gastrointestinal tract Laryngeal cleft Generalized ichthyosis Hypoplasia of the frontal lobes Optic nerve dysplasia Patchy alopecia Abnormal tricuspid valve morphology Anterior creases of earlobe Deep palmar crease Abnormality of the pulmonary artery Gastrointestinal dysmotility Abnormal mitral valve morphology Slow-growing hair Thickened helices Subvalvular aortic stenosis Hyperextensibility of the finger joints Excessive wrinkled skin Frontal balding Abnormality of hair texture Cavernous hemangioma Multiple lentigines Sparse or absent eyelashes Increased nuchal translucency Endocarditis Absent eyebrow Chronic otitis media Scarring Pachygyria Progressive visual loss Growth hormone deficiency Overgrowth Dental malocclusion Premature birth Intestinal malrotation Hypertrichosis Nevus Full cheeks Abdominal distention Palmoplantar keratoderma Sleep disturbance High, narrow palate Hepatic steatosis Retinal dystrophy Narrow forehead Joint contracture of the hand Short ribs Neurological speech impairment Pruritus Nail dystrophy Abnormality of the cerebral white matter Hoarse voice Tall stature Bulbous nose Genu valgum Dry skin Ichthyosis Peripheral axonal neuropathy Long face Broad thumb Abnormality of the cardiovascular system Cardiomegaly Melanocytic nevus Hemangioma Talipes equinovarus Clinodactyly Scaling skin Sparse eyebrow Brittle hair Redundant skin Mandibular prognathia Retrognathia Relative macrocephaly Palmoplantar hyperkeratosis Optic nerve hypoplasia Delayed gross motor development Abnormality of the genitourinary system Sleep apnea Aplasia/Hypoplasia of the corpus callosum Coarctation of aorta Talipes Amenorrhea Myocardial infarction Hemiparesis Inflammatory abnormality of the skin Nail dysplasia Round face Platyspondyly Abnormal palate morphology Cerebral visual impairment Abnormality of the pinna Abnormality of the nail Camptodactyly Sparse eyelashes Neonatal hypotonia Unilateral radial aplasia


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