Lymphoma, and Falls

Diseases related with Lymphoma and Falls

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


Top matches:

Medium match RENAL CELL CARCINOMA, NONPAPILLARY; RCC


The Heidelberg histologic classification of renal cell tumors subdivides renal cell tumors into benign and malignant parenchymal neoplasms and, where possible, limits each subcategory to the most common documented genetic abnormalities (Kovacs et al., 1997). Malignant tumors are subclassified into common or conventional renal cell carcinoma (clear cell); papillary renal cell carcinoma; chromophobe renal cell carcinoma; collecting duct carcinoma, with medullary carcinoma of the kidney; and unclassified renal cell carcinoma. The common or conventional type accounts for about 75% of renal cell neoplasms and is characterized genetically by a highly specific deletion of chromosome 3p. Papillary renal cell carcinoma (see {605074}) accounts for about 10% of renal cell tumors. Chromophobe renal cell carcinoma accounts for approximately 5% of renal cell neoplasms. Genetically, chromophobe RCC is characterized by a combination of loss of heterozygosity of chromosomes 1, 2, 6, 10, 13, 17, and 21 and hypodiploid DNA content. Collecting duct carcinoma accounts for about 1% of renal cell carcinoma.Renal cell carcinoma occurs nearly twice as often in men as in women; incidence in the United States is equivalent among whites and blacks. Cigarette smoking doubles the likelihood of renal cell carcinoma and contributes to as many as one-third of cases. Obesity is also a risk factor, particularly in women. Other risk factors include hypertension, unopposed estrogen therapy, and occupational exposure to petroleum products, heavy metals, or asbestos (summary by Motzer et al., 1996). Genetic Heterogeneity of Renal Cell CarcinomaGermline mutation resulting in nonpapillary renal cell carcinoma of the clear cell and chromophobe type occurs in the HNF1A gene (OMIM ) and the HNF1B gene (OMIM ).Somatic mutations in renal cell carcinomas occur in the VHL gene (OMIM ), the TRC8 gene (OMIM ), the OGG1 gene (OMIM ), the ARMET gene (OMIM ), the FLCN gene (OMIM ), and the BAP1 gene (OMIM ).See also RCCX1 (OMIM ) for a discussion of renal cell carcinoma associated with translocations of chromosome Xp11.2 involving the TFE3 gene (OMIM ).For a discussion of papillary renal cell carcinoma, see RCCP1 (OMIM ). Occurrence of Renal Cell Carcinoma in Other DisordersVon Hippel-Lindau syndrome (OMIM ) is a familial multicancer syndrome in which there is a susceptibility to a variety of neoplasms, including renal cell carcinoma of clear cell histology and renal cysts. A syndrome of predisposition to uterine leiomyomas and papillary renal cell carcinoma has been reported (OMIM ). Medullary carcinoma of the kidney is believed to arise from the collecting ducts of the renal medulla and is associated with sickle cell trait (OMIM ) (Kovacs et al., 1997). Renal cell carcinoma occurs in patients with the Birt-Hogg-Dube syndrome (OMIM ).Bertolotto et al. (2011) identified a missense mutation in the MITF (OMIM ) gene that increases the risk of renal cell carcinoma with or without malignant melanoma (CMM8 ).

RENAL CELL CARCINOMA, NONPAPILLARY; RCC Is also known as hypernephroma|adenocarcinoma of kidney

Related symptoms:

  • Neoplasm
  • Hypertension
  • Obesity
  • Carcinoma
  • Falls


SOURCES: OMIM ORPHANET MENDELIAN

More info about RENAL CELL CARCINOMA, NONPAPILLARY; RCC

Medium match X-LINKED LYMPHOPROLIFERATIVE DISEASE


X-linked lymphoproliferative disease is a hereditary immunodeficiency characterized, in the majority of cases, by an inadequate immune response to infection with the Epstein-Barr virus (EBV).

X-LINKED LYMPHOPROLIFERATIVE DISEASE Is also known as xlpd|duncan disease|xlp|immunodeficiency 5|infectious mononucleosis, severe, susceptibility to|purtilo syndrome|imd5|ebvs|lymphoproliferative disease, x-linked|epstein-barr virus infection, familial fatal|lyp|ebv infection, severe, susceptibility to|immun

Related symptoms:

  • Seizures
  • Neoplasm
  • Anemia
  • Hepatomegaly
  • Fever


SOURCES: ORPHANET OMIM MENDELIAN

More info about X-LINKED LYMPHOPROLIFERATIVE DISEASE

Medium match CHÉDIAK-HIGASHI SYNDROME


Chédiak-Higashi syndrome (CHS) is a rare severe genetic disorder generally characterized by partial oculocutaneous albinism (OCA, see this term), severe immunodeficiency, mild bleeding, neurological dysfunction and lymphoproliferative disorder. A classic, early-onset form and an attenuated, later-onset form (Atypical CHS; see this term) have been described.

CHÉDIAK-HIGASHI SYNDROME Is also known as chÉdiak-higashi-steinbrink syndrome|chÉdiak-higashi disease

Related symptoms:

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


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about CHÉDIAK-HIGASHI SYNDROME

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Other less relevant matches:

Medium 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

Medium 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

Medium match X-LINKED SIDEROBLASTIC ANEMIA


X-linked sideroblastic anemia is a constitutional microcytic, hypochromic anemia of varying severity that is clinically characterized by manifestations of anemia and iron overload and that may respond to treatment with pyridoxine and folic acid.

X-LINKED SIDEROBLASTIC ANEMIA Is also known as anemia, hereditary sideroblastic|xlsa|anemia, hypochromic|anemia, sideroblastic, x-linked|anh1|hereditary iron-loading anemia

Related symptoms:

  • Ataxia
  • Muscle weakness
  • Anemia
  • Hepatomegaly
  • Fatigue


SOURCES: ORPHANET OMIM MENDELIAN

More info about X-LINKED SIDEROBLASTIC ANEMIA

Medium match NEMALINE MYOPATHY 2; NEM2


Nemaline myopathy-2 is an autosomal recessive skeletal muscle disorder with a wide range of severity. The most common clinical presentation is early-onset (in infancy or childhood) muscle weakness predominantly affecting proximal limb muscles. Muscle biopsy shows accumulation of Z-disc and thin filament proteins into aggregates named 'nemaline bodies' or 'nemaline rods,' usually accompanied by disorganization of the muscle Z discs. The clinical and histologic spectrum of entities caused by variants in the NEB gene is a continuum, ranging in severity from the severe form with perinatal onset and fetal death to milder forms with later onset. The distribution of weakness can vary from generalized muscle weakness, more pronounced in proximal limb muscles, to distal-only involvement, although neck flexor weakness appears to be rather consistent. Histologic patterns range from a severe usually nondystrophic disturbance of the myofibrillar pattern to an almost normal pattern, with or without nemaline bodies, sometimes combined with cores (summary by Lehtokari et al., 2014).For a discussion of genetic heterogeneity of nemaline myopathy, see NEM3 (OMIM ).Mutations in the NEB gene are the most common cause of nemaline myopathy (Lehtokari et al., 2006).

Related symptoms:

  • Generalized hypotonia
  • Scoliosis
  • Hypertelorism
  • Muscle weakness
  • Cleft palate


SOURCES: OMIM MESH MENDELIAN

More info about NEMALINE MYOPATHY 2; NEM2

Low match CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A; CMT1A


For a general phenotypic description and a discussion of genetic heterogeneity of Charcot-Marie-Tooth disease type 1, see CMT1B (OMIM ).CMT1A is the most common form of CMT. The average age of onset of clinical symptoms is 12.2 +/- 7.3 years. Slow nerve conduction velocity (NCV) less than 38 m/s is highly diagnostic and is a 100% penetrant phenotype independent of age ({36,39:Lupski et al., 1991, 1992}).

CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A; CMT1A Is also known as hereditary motor and sensory neuropathy ia|hmsn ia|charcot-marie-tooth neuropathy, type 1a|hmsn1a|charcot-marie-tooth disease, autosomal dominant, with focally folded myelin sheaths, type 1a

Related symptoms:

  • Global developmental delay
  • Hearing impairment
  • Muscle weakness
  • Motor delay
  • Peripheral neuropathy


SOURCES: OMIM MENDELIAN

More info about CHARCOT-MARIE-TOOTH DISEASE, DEMYELINATING, TYPE 1A; CMT1A

Low match HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES


Hereditary neuropathy with liability to pressure palsies (HNPP) is an inherited peripheral nerve disorder characterized by recurrent mononeuropathy usually triggered by minor physical activities.

HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES Is also known as hnpp|potato-grubbing palsy|polyneuropathy, familial recurrent|current pressure-sensitive neuropathy|heterozygous microdeletion 17p11.2p12|tulip-bulb digger's palsy|tomaculous neuropathy

Related symptoms:

  • Hearing impairment
  • Scoliosis
  • Muscle weakness
  • Pain
  • Peripheral neuropathy


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about HEREDITARY NEUROPATHY WITH LIABILITY TO PRESSURE PALSIES

Low match X-LINKED RETINOSCHISIS


X-linked retinoschisis (XLRS) is a genetic ocular disease that is characterized by reduced visual acuity in males due to juvenile macular degeneration.

X-LINKED RETINOSCHISIS Is also known as rs|x-linked juvenile retinoschisis|xlrs|xlrs1

Related symptoms:

  • Nystagmus
  • Strabismus
  • Cataract
  • Visual impairment
  • Blindness


SOURCES: OMIM ORPHANET MENDELIAN

More info about X-LINKED RETINOSCHISIS

Top 5 symptoms//phenotypes associated to Lymphoma and Falls

Symptoms // Phenotype % cases
Splenomegaly Uncommon - Between 30% and 50% cases
Neoplasm Uncommon - Between 30% and 50% cases
Hepatomegaly Uncommon - Between 30% and 50% cases
Abnormality of the eye Uncommon - Between 30% and 50% cases
Hyporeflexia Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Areflexia Edema Strabismus Generalized hypotonia Global developmental delay Hyperpigmentation of the skin Hepatosplenomegaly Thrombocytopenia Foot dorsiflexor weakness Muscle weakness Hypertelorism Long philtrum Peripheral neuropathy Skeletal muscle atrophy Downslanted palpebral fissures Polyhydramnios Atrial septal defect Motor delay Hypermetropia Feeding difficulties Hodgkin lymphoma Low-set ears Ataxia Cryptorchidism Leukemia Nystagmus Bruising susceptibility Abnormal bleeding Abnormality of vision Seizures Anemia Hearing impairment Peripheral demyelination Scoliosis Sensory neuropathy

Rare Symptoms - Less than 30% cases


Generalized muscle weakness Optic atrophy Hypertension Sleep apnea Cranial nerve paralysis Failure to thrive Frontal bossing Limb muscle weakness Retinal dystrophy Muscular hypotonia Short stature Macrocephaly Ptosis Neurofibromas Progressive visual loss Epicanthus Growth delay Depressed nasal bridge Delayed speech and language development Decreased nerve conduction velocity Melanocytic nevus Generalized hyperpigmentation Inability to walk Delayed gross motor development Myopathy Blindness Poor suck Webbed neck Respiratory insufficiency Low posterior hairline Fine hair Cafe-au-lait spot Lymphedema Hydrops fetalis Deep philtrum High palate Joint hypermobility Failure to thrive in infancy Bilateral ptosis Cataract Pleural effusion Cubitus valgus Neurodevelopmental delay Short attention span Hypochromic microcytic anemia Thick vermilion border Astigmatism Dysphagia Dysarthria Short neck Cardiomyopathy Fatigue Abnormality of cardiovascular system morphology Pectus excavatum Inguinal hernia Posteriorly rotated ears Prominent forehead High forehead Abnormality of the foot Macrotia Distal muscle weakness Low-set, posteriorly rotated ears Feeding difficulties in infancy Sparse hair Pectus carinatum Apnea Pulmonic stenosis Gastroesophageal reflux Anteverted nares Polyneuropathy B-cell lymphoma Peripheral axonal neuropathy Paresthesia Abnormality of movement Hemiparesis Hammertoe Pancytopenia Decreased motor nerve conduction velocity Axonal loss Reduced visual acuity Lymphadenopathy Vasculitis Gait disturbance Segmental peripheral demyelination/remyelination Immunodeficiency Visual impairment Intellectual disability Fever Epistaxis Burkitt lymphoma Pes cavus Abnormal aortic valve morphology Slow-growing hair Thickened helices Anterior creases of earlobe Frontal balding Subvalvular aortic stenosis Increased nuchal translucency Hyperextensibility of the finger joints Endocarditis Sparse or absent eyelashes Abnormality of the pulmonary artery Multiple lentigines Excessive wrinkled skin Cavernous hemangioma Abnormality of hair texture Severe hydrops fetalis Optic nerve dysplasia Abnormality of the optic disc Vitreous hemorrhage Macular atrophy 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 Retinal atrophy Puberty and gonadal disorders Retinal pigment epithelial atrophy Leukocoria Abnormal tricuspid valve morphology Abnormal location of ears Retinoschisis Abnormality of the hairline Hyperkeratosis pilaris Tongue thrusting Functional abnormality of the gastrointestinal tract Foveal atrophy Laryngeal cleft Generalized ichthyosis Hypoplasia of the frontal lobes Abnormal mitral valve morphology Patchy alopecia Leakage of dye on fundus fluorescein angiography Dystrophic fingernails Gastrointestinal dysmotility Obsessive-compulsive behavior Long palpebral fissure Abnormality of the sternum Infantile spasms Electronegative electroretinogram Aplasia/Hypoplasia of the eyebrow Hydroureter Malnutrition Mizuo phenomenon Open bite Large for gestational age Absent eyebrow Heart murmur Multiple cafe-au-lait spots Chronic otitis media Ectropion Scaling skin Sparse eyebrow Brittle hair Redundant skin Hyperextensible skin Relative macrocephaly Palmoplantar hyperkeratosis Optic nerve hypoplasia Macular schisis Abnormal heart valve morphology Biparietal narrowing Deep palmar crease Premature skin wrinkling Abnormality of refraction Abnormal myocardium morphology Delayed CNS myelination Abnormality of the testis Abnormality of the optic nerve Dyspnea Abnormal hair pattern Thick upper lip vermilion Woolly hair Abnormality of the gastrointestinal tract Abnormality of the ulna Hypoplasia of the zygomatic bone Curly hair Absent eyelashes Enlarged kidney Arnold-Chiari type I malformation Abnormal eyelash morphology Alopecia of scalp Atopic dermatitis Poor appetite Underdeveloped supraorbital ridges Anal stenosis Moderate vision loss Submucous cleft hard palate Abnormal retinal morphology Macrocytic anemia Elevated hepatic transaminase Progressive muscle weakness EMG: myopathic abnormalities Respiratory insufficiency due to muscle weakness Large fontanelles Frequent falls Decreased fetal movement Waddling gait Distal sensory impairment Delayed myelination Talipes Split hand Steppage gait Pterygium Arthrogryposis multiplex congenita Decreased number of peripheral myelinated nerve fibers Onion bulb formation Demyelinating peripheral neuropathy Hypopnea Axonal regeneration Muscular dystrophy Ulnar claw Hypertrophic nerve changes Myelin outfoldings Adducted thumb Congenital contracture Progressive distal muscular atrophy Distal amyotrophy Transient myeloproliferative syndrome Multiple pterygia Hand clenching Mitochondrial depletion Late-onset distal muscle weakness Kyphoscoliosis Neck flexor weakness Abnormality of the rib cage Slender build Type 1 muscle fiber predominance Nemaline bodies Akinesia Fetal akinesia sequence EMG: neuropathic changes Cystic hygroma Spinal rigidity Bulbar palsy Pericardial effusion Mildly elevated creatine phosphokinase Multiple joint contractures Myopathic facies Rocker bottom foot Abnormal nervous system electrophysiology Cold-induced muscle cramps Pallor Macular degeneration Brachial plexus neuropathy Visual loss Cleft palate Thiamine-responsive megaloblastic anemia Hypolipidemia Abnormality of iron homeostasis Glaucoma Sideroblastic anemia Abnormality of eye movement Retinal detachment Hypocholesterolemia Myelin tomacula Anemia of inadequate production Megaloblastic anemia Calf muscle pseudohypertrophy Microcytic anemia Glucose intolerance Myelodysplasia Cone/cone-rod dystrophy Cirrhosis Abnormal electroretinogram Vertigo Flexion contracture Talipes equinovarus Pain Back pain Myoclonus Weight loss Abnormality of the nervous system Paralysis Confusion Muscle cramps Hypotelorism Tetraparesis Hyperlordosis Hoarse voice Abnormality of the voice Vocal cord paresis Axonal degeneration Vocal cord paralysis Constrictive median neuropathy Low back pain Abnormal myelination Facial palsy Proximal muscle weakness Neonatal hypotonia Micropenis Hypospadias Abnormality of the genitourinary system Osteopenia Hemangioma Skin ulcer Fair hair Periodontitis Gingivitis Iris hypopigmentation Gingival bleeding Hypopigmentation of hair Resting tremor Sensory axonal neuropathy Cerebral hemorrhage Albinism Leukopenia Amblyopia White hair Hypertriglyceridemia Cutaneous photosensitivity Abnormality of extrapyramidal motor function Bradykinesia Gastrointestinal hemorrhage Brain atrophy Parkinsonism Hypopigmentation of the skin Neutropenia Neurodegeneration Paraplegia Generalized hypopigmentation Spinocerebellar tract degeneration Developmental regression Generalized hypopigmentation of hair Esotropia Triangular face Ascites Highly arched eyebrow Broad forehead Postnatal growth retardation Joint laxity Respiratory distress Cognitive impairment Abnormal facial shape Microcephaly Recurrent systemic pyogenic infections Hemophagocytosis Abnormality of multiple cell lineages in the bone marrow Giant melanosomes in melanocytes Recurrent cutaneous abscess formation Abnormal leukocyte morphology Hypofibrinogenemia Oculogyric crisis Recurrent bacterial skin infections Macular hypoplasia Partial albinism Hypersplenism Progressive peripheral neuropathy Spastic paraplegia Mental deterioration Hip dysplasia Small cell lung carcinoma Bone marrow hypocellularity Meningitis Bronchiectasis Memory impairment Decreased antibody level in blood Hepatic failure Respiratory failure Pneumonia Dilatation Hemangioblastoma Cerebellar hemangioblastoma Clear cell renal cell carcinoma Sarcoma Fibrosarcoma Papillary renal cell carcinoma Retinoblastoma Renal neoplasm Renal cell carcinoma Polycythemia Nephroblastoma Melanoma Renal cyst Carcinoma Obesity Encephalitis Increased antibody level in blood Rigidity Hepatic necrosis Photophobia Difficulty walking Jaundice Recurrent respiratory infections Recurrent infections Cerebellar atrophy Tremor Fulminant hepatitis Reduced natural killer cell activity Pharyngitis Non-Hodgkin lymphoma Pure red cell aplasia IgG deficiency Dysgammaglobulinemia Increased IgM level Chorioretinitis Granulomatosis Hepatic encephalopathy Histiocytosis Lymphocytosis Cellular immunodeficiency Recurrent pharyngitis Immune dysregulation Aplastic anemia Agammaglobulinemia Wide intermamillary distance Cyanosis Aplasia/Hypoplasia of the corpus callosum Pruritus Hepatic steatosis Bulbous nose Long face Abnormality of skin pigmentation Ichthyosis Dry skin Genu valgum Hypotrichosis Abnormality of the cerebral white matter Dolichocephaly Nail dystrophy Neurological speech impairment Sleep disturbance Abnormal cardiac septum morphology Scarring Erythema Respiratory tract infection Irritability Abnormality of the kidney Telecanthus Hypertrophic cardiomyopathy Aggressive behavior Hydronephrosis EEG abnormality High, narrow palate Palmoplantar keratoderma Coarse facial features Inflammatory abnormality of the skin Abnormal palate morphology Cutis laxa Oculomotor apraxia Sparse eyelashes Narrow palate Abnormality of the nail Aspiration Cerebral visual impairment Thickened skin Decreased body weight Open mouth Myocardial infarction Abdominal distention Coarctation of aorta Cardiomegaly Narrow forehead Abnormality of the cardiovascular system Growth hormone deficiency Dental malocclusion Premature birth Intestinal malrotation Vesicoureteral reflux Nevus Full cheeks Umbilical hernia Proptosis Mitral regurgitation Abnormality of the spleen 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 Prominent fingertip pads Chylothorax Hydrocele testis Reduced factor X activity Facial hypotonia Abnormal eyebrow morphology Decreased muscle mass Proximal placement of thumb Overfolded helix Abnormality of the thorax Cholelithiasis Bicuspid aortic valve Torticollis Bilateral single transverse palmar creases Aortic valve stenosis Reduced prothrombin activity Abnormality of the subarachnoid space Autism Cerebral atrophy Hyperkeratosis Cerebral cortical atrophy Hyperhidrosis Alopecia Constipation Clinodactyly of the 5th finger Delayed skeletal maturation Abnormal heart morphology Encephalopathy Depressivity Hernia Malar flattening Micrognathia Short nose Kyphosis Behavioral abnormality Congestive heart failure Hypertonia Abnormality of the dentition Vomiting Intellectual disability, severe Hydrocephalus Ventriculomegaly Ventricular septal defect Myopia Peripheral cystoid retinal degeneration



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