Lymphoma, and Inguinal hernia

Diseases related with Lymphoma and Inguinal hernia

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

Top matches:

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

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

Other less relevant matches:

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

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

Jacobsen syndrome is a multiple congenital anomaly/mental retardation (MCA/MR) contiguous gene syndrome caused by partial deletion of the long arm of chromosome 11.

JACOBSEN SYNDROME Is also known as monosomy 11qter|del(11)(q23.3)|distal deletion 11q|telomeric deletion 11q|distal monosomy 11q|del(11)(qter)|chromosome 11q deletion syndrome|partial 11q monosomy syndrome

Related symptoms:

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


SOURCES: OMIM ORPHANET MENDELIAN

More info about JACOBSEN SYNDROME

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

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

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

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

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

Symptoms // Phenotype % cases
Strabismus Common - Between 50% and 80% cases
Hypertelorism Common - Between 50% and 80% cases
Scoliosis Common - Between 50% and 80% cases
Thrombocytopenia Common - Between 50% and 80% cases
Intellectual disability Common - Between 50% and 80% cases

Other less frequent symptoms

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

Common Symptoms - More than 50% cases

Global developmental delay

Uncommon Symptoms - Between 30% and 50% cases

Leukemia

Common Symptoms - More than 50% cases

Bruising susceptibility

Uncommon Symptoms - Between 30% and 50% cases

Growth delay

Common Symptoms - More than 50% cases

Umbilical hernia

Uncommon Symptoms - Between 30% and 50% cases

Failure to thrive

Common Symptoms - More than 50% cases

Epicanthus

Uncommon Symptoms - Between 30% and 50% cases

Depressed nasal bridge

Common Symptoms - More than 50% cases

Cryptorchidism

Uncommon Symptoms - Between 30% and 50% cases

Frontal bossing

Common Symptoms - More than 50% cases

Prominent forehead

Uncommon Symptoms - Between 30% and 50% cases

Abnormal facial shape Short stature Downslanted palpebral fissures Macrocephaly Muscular hypotonia Micrognathia Hearing impairment Generalized hypotonia Seizures Abnormality of cardiovascular system morphology Atrial septal defect Microcephaly Astigmatism Postnatal growth retardation Low-set, posteriorly rotated ears Ptosis Short neck Ventricular septal defect Feeding difficulties Optic atrophy Anteverted nares Abnormal cardiac septum morphology Neoplasm Hydrocephalus Abnormal heart morphology Hernia Behavioral abnormality Long philtrum Congestive heart failure Myopia Joint hypermobility Ventriculomegaly Pes planus Irritability Abnormality of the dentition Clinodactyly of the 5th finger Short nose Talipes equinovarus Constipation Webbed neck Proptosis Facial asymmetry Anal atresia Hydronephrosis Acute lymphoblastic leukemia High palate Cataract Neurological speech impairment Gastroesophageal reflux Thick vermilion border Cafe-au-lait spot Neutropenia Hypospadias Feeding difficulties in infancy Anemia High forehead Abnormality of the skeletal system Delayed speech and language development Pectus excavatum Failure to thrive in infancy Edema Intrauterine growth retardation Motor delay Ataxia Nystagmus Low-set ears Abnormality of the kidney Abnormal bleeding Clinodactyly Pes cavus Sparse hair Short thumb Broad forehead Macrotia Lymphedema Kyphosis Pancytopenia Abnormal palate morphology Fine hair Dolichocephaly

Rare Symptoms - Less than 30% cases

Upslanted palpebral fissure Poor suck Neurodevelopmental delay Short attention span B-cell lymphoma Hypopigmentation of the skin Pleural effusion Bilateral ptosis Aganglionic megacolon Cubitus valgus Aplasia/Hypoplasia of the corpus callosum Multiple cafe-au-lait spots Hyperpigmentation of the skin Wide intermamillary distance Myelodysplasia Cyanosis Ectropion Epistaxis Low posterior hairline Hydroureter Deep philtrum Aortic valve stenosis Aplasia/Hypoplasia of the eyebrow Abnormality of vision Heart murmur Sleep apnea Abnormal localization of kidney Abnormal vertebral morphology Abnormal eyelash morphology Open mouth Thickened helices Aplasia/Hypoplasia of the radius Autism Absent radius Abnormality of skin pigmentation Osteopenia Coarse facial features Absent thumb Hypopigmented skin patches Aggressive behavior Hypertrophic cardiomyopathy Telecanthus Abnormality of the testis Abnormality of the eye Tracheoesophageal fistula Abnormality of the ulna Encephalopathy Prominent nasal bridge Premature birth Coarctation of aorta Hypoplasia of the ulna Narrow forehead Growth hormone deficiency Prominent nose Hepatomegaly Fever Cerebral atrophy Intestinal malrotation Vesicoureteral reflux Chromosome breakage Intellectual disability, severe Full cheeks Abdominal distention Sleep disturbance Abnormal aortic valve morphology Fatigue Toe syndactyly Craniosynostosis Spasticity Overlapping toe Flexion contracture Patent ductus arteriosus Dysarthria Hypertonia Agenesis of corpus callosum Giant platelets Hypogonadism Hypothyroidism Azoospermia Pachygyria Intellectual disability, moderate Prominent fingertip pads Microphthalmia Horseshoe kidney Bone marrow hypocellularity Skin rash Finger syndactyly Small for gestational age Spina bifida Hip dislocation Acute myeloid leukemia Hydrocele testis Diastasis recti Single transverse palmar crease Cutis laxa Flat occiput Eczema Talipes Large for gestational age Pectus carinatum Joint laxity Cardiomyopathy Splenomegaly Abnormality of the foot Respiratory distress Acute monocytic leukemia Retrognathia Trigonocephaly Hyperextensible skin Mandibular prognathia Falls Pulmonic stenosis Hypermetropia Camptodactyly Abnormality of the pinna Hyperhidrosis Posteriorly rotated ears Delayed skeletal maturation Cleft palate Polyhydramnios Wide nasal bridge Retinal dysplasia Slender finger Hearing abnormality Chronic constipation External ear malformation Meckel diverticulum Irregular hyperpigmentation Duodenal atresia Ectopic anus Abnormality of blood and blood-forming tissues Myeloid leukemia Ectopic kidney Eyelid coloboma Double outlet right ventricle Duplicated collecting system Wheezing Abnormality of the hypothalamus-pituitary axis Abnormality of femur morphology Bicornuate uterus Abnormality of the thumb Abnormality of the uterus Aplastic anemia Abnormality of the upper limb Natal tooth Abnormality of chromosome stability Duodenal stenosis Reticulocytopenia Abnormal aortic morphology Abnormality of nervous system morphology Bipolar affective disorder Primary hypothyroidism Arteriovenous malformation Abnormal eyelid morphology Abnormal renal morphology Missing ribs Transposition of the great arteries Visual impairment Squamous cell carcinoma Carcinoma Abnormality of the genital system Choanal atresia Short palpebral fissure Oligohydramnios Sloping forehead Tetralogy of Fallot Renal agenesis Vertigo Abnormality of the liver Abnormality of the anus Annular pancreas Weight loss Telangiectasia Internal hemorrhage Diabetes mellitus Severe short stature Headache Arteria lusoria Renal insufficiency Bilateral camptodactyly Congenital thrombocytopenia Megakaryocyte dysplasia Hyperreflexia Abnormality of the curvature of the vertebral column Recurrent urinary tract infections Insulin resistance Mitral stenosis Long hallux Broad hallux phalanx Glucose intolerance Nuclear cataract Triphalangeal thumb Hyperinsulinemia Aplasia/Hypoplasia of the earlobes Labial hypoplasia Abnormal thrombocyte morphology Broad columella Nasolacrimal duct obstruction Abnormality of the head Abnormality of the urinary system Toe clinodactyly Reduced bone mineral density Urethral stenosis Renal hypoplasia/aplasia Cranial nerve paralysis U-Shaped upper lip vermilion Leukopenia Type I diabetes mellitus Central hypothyroidism Clitoral hypoplasia Macular hypoplasia Hypergonadotropic hypogonadism Low-grade fever Oligodactyly Aplasia/Hypoplasia of the iris Specific learning disability Short philtrum Severe global developmental delay Thick eyebrow Small hand Tapered finger Convex nasal ridge Thick lower lip vermilion Upper limb undergrowth Postnatal microcephaly Truncal ataxia Abnormal autonomic nervous system physiology Finger clinodactyly Intellectual disability, progressive Widely spaced teeth Mutism Lower limb hyperreflexia Short 4th metacarpal Incoordination Anxiety Hypoplasia of the corpus callosum Absent speech Pneumonia Micropenis Gait ataxia Deeply set eye Apnea Abnormality of chromosome segregation Protruding ear Median cleft palate Lower limb hypertonia Autistic behavior Ectopic calcification Short 5th metacarpal Wide mouth Coarse hair Short metatarsal Aphalangy of the hands Triangular nasal tip Square face Small cerebral cortex Failure of eruption of permanent teeth Narrow foot Intermittent hyperventilation Broad fingertip Overhanging nasal tip Happy demeanor Polydactyly Skeletal dysplasia Generalized tonic-clonic seizures Recurrent otitis media Gingival overgrowth Foot dorsiflexor weakness Mild short stature Large beaked nose Pes valgus Self-injurious behavior Hyperventilation Clubbing Cupped ear Supernumerary nipple Aphasia Dysphasia Hodgkin lymphoma Hiatus hernia Abnormal pattern of respiration Acrocyanosis Esophagitis Misalignment of teeth Echolalia Clubbing of fingers Abnormality of the helix Breathing dysregulation Unilateral radial aplasia Anomalous splenoportal venous system Complete duplication of thumb phalanx Bowing of the long bones Conductive hearing impairment Malabsorption Polymicrogyria Bifid uvula Underdeveloped nasal alae Hypotelorism Renal dysplasia Brachycephaly Large fontanelles Narrow face Spina bifida occulta Abnormality of the metacarpal bones Hypoplasia of the radius Hallux valgus Narrow nasal bridge Narrow mouth Abnormality of the preputium Aplasia/Hypoplasia of the thumb Compensated hypothyroidism Partial duplication of thumb phalanx Clubbing of toes Decreased fertility in males Chromosomal breakage induced by crosslinking agents Hypoplastic anemia Absent testis Almond-shaped palpebral fissure Pyridoxine-responsive sideroblastic anemia Abnormal carotid artery morphology 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 Aplasia/Hypoplasia of fingers Anteriorly placed anus Short humerus Midface capillary hemangioma Urogenital fistula Lambdoidal craniosynostosis Aplasia/Hypoplasia of the patella Ulnar bowing Brachyturricephaly Metopic synostosis Abnormality of the carpal bones Flat forehead Hand oligodactyly Bilateral radial aplasia Aplasia of metacarpal bones Bicoronal synostosis Perineal fistula Limited shoulder movement Persistent cloaca Carpal bone aplasia Limited elbow movement Patellar hypoplasia Hyposegmentation of neutrophil nuclei Osteosarcoma Fibular hypoplasia Abnormality of the ureter Carpal synostosis Shallow orbits Coronal craniosynostosis Choanal stenosis Atrioventricular canal defect Anterior plagiocephaly Rectovaginal fistula Poikiloderma Rib fusion Bilateral conductive hearing impairment Sagittal craniosynostosis Folate deficiency Oxycephaly Partial agenesis of the corpus callosum Sparse or absent eyelashes Hypoplastic left heart Abnormal eyebrow morphology Juvenile myelomonocytic leukemia Reduced factor XII activity Hypoplasia of olfactory tract Reduced factor IX activity Abnormality of the mediastinum Arteritis Pulmonary lymphangiectasia Monocytosis Broad toe Chylothorax Hypochromic microcytic anemia Abnormality of the spleen Facial hypotonia Decreased muscle mass Reduced factor X activity Proximal placement of thumb Overfolded helix Abnormality of the thorax Cholelithiasis Bicuspid aortic valve Torticollis Vasculitis Bilateral single transverse palmar creases Hydrops fetalis Mitral regurgitation Hip dysplasia Esotropia Triangular face Ascites Reduced prothrombin activity Abnormality of the subarachnoid space Hepatosplenomegaly Genu valgum Abnormality of the cardiovascular system Progressive visual loss Dental malocclusion Nevus Palmoplantar keratoderma High, narrow palate Hepatic steatosis Retinal dystrophy Bulbous nose Long face Peripheral axonal neuropathy Ichthyosis Dry skin Hypotrichosis Dysphagia Abnormality of the cerebral white matter Nail dystrophy Pruritus Scarring Erythema Respiratory tract infection EEG abnormality Hyperkeratosis Cerebral cortical atrophy Alopecia Depressivity Malar flattening Vomiting Blindness Highly arched eyebrow Myopathy Myocardial infarction Overgrowth Radial deviation of finger Large hands Back pain Slurred speech Accelerated skeletal maturation Coxa valga Pointed chin Short ribs Hoarse voice Joint contracture of the hand Tall stature Broad thumb Hypertrichosis Amenorrhea Bilateral talipes equinovarus Nail dysplasia Round face Platyspondyly Neonatal hypotonia Pain Gingival recession Periodontitis Premature loss of teeth Gingival bleeding Fragile skin Atrophic scars Nephroblastoma Osteoarthritis Arthralgia Metatarsus adductus Limited elbow extension Gait disturbance Galactorrhea Hypertension Cognitive impairment Dysharmonic bone age Flared humeral metaphysis Abnormally low-pitched voice Limited knee extension Flared femoral metaphysis Lumbar kyphosis Sacrococcygeal teratoma Deep-set nails Horizontal eyebrow Vertebral wedging Short fourth metatarsal Teratoma Absent septum pellucidum Thin nail Thoracolumbar kyphosis Calcaneovalgus deformity Poor fine motor coordination Dimple chin Broad philtrum Dilation of lateral ventricles Broad face Large earlobe Hypoplastic iliac wing Down-sloping shoulders Prolactin excess Inverted nipples Secondary amenorrhea Cardiomegaly Hemiparesis Hammertoe Inappropriate crying Brachydactyly Sensorineural hearing impairment Refractory anemia Impaired platelet aggregation Acute leukemia Neuroblastoma Prolonged bleeding time Purpura Oral aversion Multiple plantar creases Eyelid fasciculation Multiple palmar creases Abnormality of the auditory canal Cutaneous T-cell lymphoma Syndactyly Morphological abnormality of the gastrointestinal tract Puberty and gonadal disorders Abnormal location of ears Abnormality of the hairline Hyperkeratosis pilaris 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 Abnormality of the optic disc Intellectual disability, mild Immunodeficiency Frontal balding Dehydration Chorioretinal coloboma Hand polydactyly Pyloric stenosis Schizophrenia Infantile muscular hypotonia Tachypnea Holoprosencephaly Multicystic kidney dysplasia Leukodystrophy Short toe Sinusitis Amblyopia Abnormal form of the vertebral bodies Microdontia Recurrent infections Otitis media Decreased antibody level in blood Postural instability Microcornea Iris coloboma Tachycardia Smooth philtrum Narrow chest Attention deficit hyperactivity disorder Coloboma Hypoglycemia Thin upper lip vermilion Osteoporosis Recurrent respiratory infections Anterior creases of earlobe Endocarditis Inflammatory abnormality of the skin Brittle hair Abnormal heart valve morphology Long palpebral fissure Abnormality of the sternum Infantile spasms Neurofibromas Malnutrition Open bite Absent eyebrow Obsessive-compulsive behavior Chronic otitis media Melanocytic nevus Scaling skin Sparse eyebrow Redundant skin Curly hair Relative macrocephaly Palmoplantar hyperkeratosis Optic nerve hypoplasia Delayed gross motor development Abnormality of the genitourinary system Hemangioma Oculomotor apraxia Sparse eyelashes Narrow palate Abnormality of the nail Aspiration Cerebral visual impairment Thickened skin Decreased body weight Biparietal narrowing Generalized hyperpigmentation Increased nuchal translucency Abnormality of the optic nerve Multiple lentigines Cavernous hemangioma Abnormality of hair texture Excessive wrinkled skin Abnormality of the pulmonary artery Hyperextensibility of the finger joints Subvalvular aortic stenosis Slow-growing hair Abnormal mitral valve morphology Gastrointestinal dysmotility Deep palmar crease Abnormality of refraction Abnormal myocardium morphology Delayed CNS myelination Dystrophic fingernails Submucous cleft hard palate Abnormal hair pattern Thick upper lip vermilion Woolly hair Abnormality of the gastrointestinal tract Premature skin wrinkling Hypoplasia of the zygomatic bone Absent eyelashes Enlarged kidney Arnold-Chiari type I malformation Alopecia of scalp Atopic dermatitis Poor appetite Underdeveloped supraorbital ridges Anal stenosis Short 3rd metacarpal


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