Lymphoma, and Hernia

Diseases related with Lymphoma and Hernia

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


Top matches:

Low match PLATELET DISORDER, FAMILIAL, WITH ASSOCIATED MYELOID MALIGNANCY; FPDMM


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

Low match EHLERS-DANLOS SYNDROME, PERIODONTAL TYPE, 2; EDSPD2


Related symptoms:

  • Scoliosis
  • Neoplasm
  • Fever
  • Inguinal hernia
  • Arthralgia


SOURCES: OMIM MENDELIAN

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

Low match PITT-HOPKINS 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

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Other less relevant matches:

Low 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

Low match NOONAN SYNDROME-LIKE DISORDER WITH JUVENILE MYELOMONOCYTIC LEUKEMIA


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

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 CARDIOFACIOCUTANEOUS SYNDROME


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

Low match PELGER-HUET ANOMALY; PHA


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 SYSTEMIC MASTOCYTOSIS WITH AN ASSOCIATED CLONAL HEMATOLOGIC NON-MAST CELL LINEAGE DISEASE


Systemic mastocytosis with an associated clonal hematological non-mast cell lineage disease is a form of systemic mastocytosis (SM) associated with malignancy (other than mast cell leukemia).

SYSTEMIC MASTOCYTOSIS WITH AN ASSOCIATED CLONAL HEMATOLOGIC NON-MAST CELL LINEAGE DISEASE Is also known as systemic mastocytosis with associated hematologic neoplasm|sm-ahnmd|sm-ahn

Related symptoms:

  • Eosinophilia
  • Myelodysplasia
  • Acute myeloid leukemia
  • Chronic myelogenous leukemia
  • Non-Hodgkin lymphoma


SOURCES: ORPHANET MENDELIAN

More info about SYSTEMIC MASTOCYTOSIS WITH AN ASSOCIATED CLONAL HEMATOLOGIC NON-MAST CELL LINEAGE DISEASE

Low match CUTIS MARMORATA TELANGIECTATICA CONGENITA


Cutis marmorata telangiectatica congenita (CMTC) is a congenital localized or generalized vascular anomaly characterized by a persistent cutis marmorata pattern with a marbled bluish to deep purple appearance, spider nevus-like telangiectasia, phlebectasia and, occasionally, ulceration and atrophy of the affected skin.

CUTIS MARMORATA TELANGIECTATICA CONGENITA Is also known as megalencephaly-cutis marmorata telangiectatica congenita|cmtc|mcmtc|megalencephaly-capillary malformation syndrome|macrocephaly-cutis marmorata telangiectatica congenita|mcm|macrocephaly-capillary malformation

Related symptoms:

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


SOURCES: OMIM ORPHANET MENDELIAN

More info about CUTIS MARMORATA TELANGIECTATICA CONGENITA

Top 5 symptoms//phenotypes associated to Lymphoma and Hernia

Symptoms // Phenotype % cases
Global developmental delay Common - Between 50% and 80% cases
Leukemia Common - Between 50% and 80% cases
Hypertelorism Common - Between 50% and 80% cases
Failure to thrive Common - Between 50% and 80% cases
Strabismus Common - Between 50% and 80% cases
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Other less frequent symptoms

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

Common Symptoms - More than 50% cases


Intellectual disability

Uncommon Symptoms - Between 30% and 50% cases


Umbilical hernia

Common Symptoms - More than 50% cases


Scoliosis

Uncommon Symptoms - Between 30% and 50% cases


Depressed nasal bridge Macrocephaly Neoplasm Generalized hypotonia Growth delay Muscular hypotonia Cryptorchidism Frontal bossing Bruising susceptibility Thrombocytopenia Epicanthus Abnormality of cardiovascular system morphology Abnormal facial shape Downslanted palpebral fissures Prominent forehead Postnatal growth retardation Seizures Thick vermilion border Edema Astigmatism Joint hypermobility Inguinal hernia Micrognathia Short neck Short stature Large for gestational age Kyphosis Low-set ears Anteverted nares Delayed speech and language development Ptosis Abnormal bleeding Long philtrum Fine hair Neutropenia Cafe-au-lait spot Pes cavus Macrotia Joint laxity Broad forehead Abnormal heart morphology Feeding difficulties Myelodysplasia Gastroesophageal reflux Hydrocephalus Irritability Atrial septal defect High forehead Multiple cafe-au-lait spots Ventriculomegaly Hearing impairment Microcephaly Ataxia Lymphedema Cutis laxa Ventricular septal defect Acute lymphoblastic leukemia Acute myeloid leukemia Sparse hair

Rare Symptoms - Less than 30% cases


Overgrowth Microphthalmia Clinodactyly of the 5th finger Abnormality of skin pigmentation Patent ductus arteriosus Hypertrophic cardiomyopathy Proptosis Vesicoureteral reflux Abnormality of the eye Dysarthria Abnormality of the kidney Polydactyly Abnormal cardiac septum morphology Finger syndactyly Dolichocephaly Hypothyroidism Toe syndactyly Nevus Hypertonia Behavioral abnormality Delayed skeletal maturation Hyperhidrosis Anemia Cubitus valgus Congestive heart failure Feeding difficulties in infancy Cardiomyopathy Deep philtrum Splenomegaly Pectus excavatum Posteriorly rotated ears Polyhydramnios Low-set, posteriorly rotated ears Pectus carinatum Poor suck Hypermetropia Pulmonic stenosis Abnormality of the foot Falls Ascites Webbed neck Low posterior hairline Respiratory distress Optic atrophy Intrauterine growth retardation Dilation of lateral ventricles Hepatomegaly High palate Cataract Nystagmus Hemangioma Hydrocele testis Large earlobe Redundant skin Cognitive impairment B-cell lymphoma Short attention span Prominent fingertip pads Neurodevelopmental delay Arnold-Chiari type I malformation Pleural effusion Bilateral ptosis Failure to thrive in infancy Thickened helices Hyperpigmentation of the skin Motor delay Fatigue Abnormality of vision Abnormality of the pinna Aganglionic megacolon Open mouth Abnormality of the testis Narrow forehead Cyanosis Coarse facial features Wide nasal bridge Wide intermamillary distance Myopia Arteriovenous malformation Clinodactyly Abnormality of the skeletal system Abnormality of the dentition Full cheeks Abdominal distention Hypopigmentation of the skin Sleep disturbance Talipes equinovarus Constipation Hydroureter Intellectual disability, severe Abnormality of the upper limb Neurological speech impairment Reduced bone mineral density Encephalopathy Abnormal palate morphology Abnormality of the ulna Pes planus Hypospadias Deeply set eye Epistaxis Telangiectasia Purpura Mandibular prognathia Autism Overlapping toe Upslanted palpebral fissure Acute monocytic leukemia Fever Hypopigmented skin patches Aplasia/Hypoplasia of the corpus callosum Sleep apnea Nephroblastoma Hyperextensible skin Abnormal aortic valve morphology Aggressive behavior Melanocytic nevus Relative macrocephaly Brittle hair Palmoplantar hyperkeratosis Prolonged G2 phase of cell cycle Optic nerve hypoplasia Ectropion Sparse eyebrow Scaling skin Dry skin Chronic otitis media Partial duplication of thumb phalanx Neurofibromas Aplasia/Hypoplasia of the eyebrow Malnutrition Open bite Absent eyebrow Low-grade fever Aplasia/Hypoplasia of the iris Complete duplication of thumb phalanx Clubbing of toes Abnormal carotid artery morphology Obsessive-compulsive behavior Decreased fertility in males Chromosomal breakage induced by crosslinking agents Hypoplastic anemia Absent testis Compensated hypothyroidism Almond-shaped palpebral fissure Heart murmur Delayed gross motor development Decreased body weight Abnormality of the genitourinary system Intestinal malrotation Depressivity Alopecia Cerebral cortical atrophy Hyperkeratosis Osteopenia EEG abnormality Hydronephrosis Telecanthus Respiratory tract infection Premature birth Erythema Scarring Dental malocclusion Pruritus Nail dystrophy Abnormality of the cerebral white matter Palmoplantar keratoderma High, narrow palate Hypotrichosis Hepatic steatosis Retinal dystrophy Bulbous nose Long face Genu valgum Cerebral atrophy Malar flattening Anemic pallor Hemiparesis Oculomotor apraxia Sparse eyelashes Narrow palate Abnormality of the nail Aspiration Cerebral visual impairment Thickened skin Ichthyosis Deficient excision of UV-induced pyrimidine dimers in DNA Inflammatory abnormality of the skin Neoplasm of head and neck Aplasia/Hypoplasia of the uvula Short nose Aplasia/Hypoplasia of fingers Myocardial infarction Pyridoxine-responsive sideroblastic anemia Abnormality of the preputium Dysphagia Coarctation of aorta Blindness Vomiting Cardiomegaly Abnormality of the cardiovascular system Progressive visual loss Growth hormone deficiency Peripheral axonal neuropathy Excessive wrinkled skin Infantile spasms Mastocytosis Shock Multicystic kidney dysplasia Postaxial hand polydactyly Abnormality of the skin Retinal detachment Postaxial polydactyly Polymicrogyria Oral cleft Smooth philtrum Stroke Abnormality of the nervous system Arrhythmia Syndactyly Chronic myelomonocytic leukemia Non-Hodgkin lymphoma Ischemic stroke Chronic myelogenous leukemia Eosinophilia Short 3rd metacarpal Hyposegmentation of neutrophil nuclei Folate deficiency Median cleft palate Giant platelets Lower limb hypertonia Ectopic calcification Short 5th metacarpal Abnormality of chromosome segregation Short 4th metacarpal Upper limb undergrowth Lower limb hyperreflexia Cutaneous syndactyly Arnold-Chiari malformation Foot dorsiflexor weakness Arterial stenosis Cutis marmorata telangiectatica congenita Vascular ring Displacement of the external urethral meatus Progressive macrocephaly Leukocoria Hemimegalencephaly Facial hemangioma Capillary malformation Short lower limbs Subcutaneous hemorrhage Perisylvian polymicrogyria Asymmetric growth Right aortic arch Skin erosion Cavum septum pellucidum Cutis marmorata Severe postnatal growth retardation Cortical dysplasia Abnormality of digit Aplasia/Hypoplasia of the skin Telangiectasia of the skin Syringomyelia Nevus flammeus Severe failure to thrive Atrial flutter Capillary hemangioma Megalencephaly Meningioma Varicose veins Abnormality of the lower limb Hemihypertrophy Mild short stature Gingival overgrowth Abnormality of the sternum Premature skin wrinkling Subvalvular aortic stenosis Slow-growing hair Abnormal mitral valve morphology Gastrointestinal dysmotility Deep palmar crease Abnormality of refraction Abnormal myocardium morphology Delayed CNS myelination Abnormality of the optic nerve Dystrophic fingernails Abnormal hair pattern Thick upper lip vermilion Woolly hair Abnormality of the gastrointestinal tract Hypoplasia of the zygomatic bone Abnormality of the pulmonary artery Absent eyelashes Enlarged kidney Abnormal eyelash morphology Alopecia of scalp Atopic dermatitis Poor appetite Underdeveloped supraorbital ridges Anal stenosis Submucous cleft hard palate Generalized hyperpigmentation Curly hair Biparietal narrowing Abnormal heart valve morphology Long palpebral fissure Hyperextensibility of the finger joints Duplicated collecting system Recurrent otitis media Hyperkeratosis pilaris Eczema Generalized tonic-clonic seizures Skeletal dysplasia Oral aversion Multiple plantar creases Eyelid fasciculation Multiple palmar creases Abnormality of the auditory canal Inappropriate crying Cutaneous T-cell lymphoma Morphological abnormality of the gastrointestinal tract Puberty and gonadal disorders Abnormal location of ears Abnormality of the hairline Tongue thrusting Abnormality of hair texture Anterior creases of earlobe Cavernous hemangioma Multiple lentigines Sparse or absent eyelashes Increased nuchal translucency Endocarditis Frontal balding Abnormality of the optic disc Functional abnormality of the gastrointestinal tract Abnormal tricuspid valve morphology Patchy alopecia Optic nerve dysplasia Hypoplasia of the frontal lobes Generalized ichthyosis Laryngeal cleft Meckel diverticulum Headache Duodenal stenosis Overhanging nasal tip Amenorrhea Nail dysplasia Round face Talipes Platyspondyly Camptodactyly Neonatal hypotonia Retrognathia Flexion contracture Spasticity Pain Triangular nasal tip Pachygyria Broad fingertip Intermittent hyperventilation Narrow foot Failure of eruption of permanent teeth Small cerebral cortex Square face Large beaked nose Happy demeanor Pes valgus Abnormal pattern of respiration Breathing dysregulation Abnormality of the helix Hypertrichosis Broad thumb Echolalia Limited elbow extension Calcaneovalgus deformity Poor fine motor coordination Dimple chin Broad philtrum Broad face Hypoplastic iliac wing Diastasis recti Down-sloping shoulders Prolactin excess Inverted nipples Secondary amenorrhea Absent septum pellucidum Bilateral talipes equinovarus Tall stature Metatarsus adductus Flat occiput 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 Clubbing of fingers Misalignment of teeth Thin nail Hypoplasia of the corpus callosum Short philtrum Wide mouth Autistic behavior Protruding ear Apnea Intellectual disability, moderate Anxiety Gait ataxia Micropenis Pneumonia Absent speech Gingival recession Severe global developmental delay Periodontitis Premature loss of teeth Gingival bleeding Fragile skin Atrophic scars Osteoarthritis Arthralgia Refractory anemia Impaired platelet aggregation Acute leukemia Neuroblastoma Prolonged bleeding time Prominent nasal bridge Thick eyebrow Esophagitis Coarse hair Acrocyanosis Hiatus hernia Hyperventilation Hodgkin lymphoma Dysphasia Aphasia Supernumerary nipple Cupped ear Clubbing Self-injurious behavior Short metatarsal Incoordination Mutism Small hand Widely spaced teeth Intellectual disability, progressive Finger clinodactyly Abnormal autonomic nervous system physiology Truncal ataxia Postnatal microcephaly Thick lower lip vermilion Specific learning disability Convex nasal ridge Prominent nose Single transverse palmar crease Tapered finger Thoracolumbar kyphosis Teratoma Primary hypothyroidism Short thumb Renal hypoplasia/aplasia Cranial nerve paralysis Azoospermia Leukopenia Type I diabetes mellitus Horseshoe kidney Bone marrow hypocellularity Hypergonadotropic hypogonadism Spina bifida Abnormal vertebral morphology Insulin resistance Recurrent urinary tract infections Hyperinsulinemia Abnormality of the genital system Choanal atresia Short palpebral fissure Pancytopenia Oligohydramnios Sloping forehead Tetralogy of Fallot Renal agenesis Vertigo Anal atresia Facial asymmetry Hip dislocation Abnormality of the urinary system Triphalangeal thumb Abnormality of the liver Abnormal eyelid morphology Abnormality of nervous system morphology Abnormal aortic morphology Reticulocytopenia Abnormality of chromosome stability Abnormal localization of kidney Abnormal renal morphology Abnormality of the hypothalamus-pituitary axis Abnormality of femur morphology Bicornuate uterus Abnormality of the thumb Abnormality of the uterus Aplastic anemia Chromosome breakage Tracheoesophageal fistula Hearing abnormality External ear malformation Irregular hyperpigmentation Aplasia/Hypoplasia of the radius Absent radius Abnormality of blood and blood-forming tissues Myeloid leukemia Absent thumb Ectopic kidney Squamous cell carcinoma Hypoplasia of the ulna Glucose intolerance Small for gestational age Carcinoma Galactorrhea Myopathy Torticollis Vasculitis Bilateral single transverse palmar creases Aortic valve stenosis Hydrops fetalis Mitral regurgitation Hip dysplasia Esotropia Triangular face Highly arched eyebrow Hepatosplenomegaly Gait disturbance Cholelithiasis Hypertension 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 Bicuspid aortic valve Abnormality of the thorax Weight loss Hypoplasia of olfactory tract Diabetes mellitus Hypogonadism Severe short stature Renal insufficiency Hyperreflexia Visual impairment Cleft palate Abnormality of the subarachnoid space Reduced factor X activity Reduced prothrombin activity Juvenile myelomonocytic leukemia Reduced factor XII activity Reduced factor IX activity Overfolded helix Abnormality of the mediastinum Arteritis Pulmonary lymphangiectasia Monocytosis Broad toe Chylothorax Hypochromic microcytic anemia Abnormality of the spleen Facial hypotonia Abnormal eyebrow morphology Decreased muscle mass Proximal placement of thumb Blue nevus



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Myopia and Cone/cone-rod dystrophy, related diseases and genetic alterations Dysarthria and Anxiety, related diseases and genetic alterations

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