Arthritis, and Constipation

Diseases related with Arthritis and Constipation

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


Top matches:

Medium match CATARACT-GLAUCOMA SYNDROME


Cataract-glaucoma syndrome is characterised by the association of total bilateral congenital cataract with the secondary occurrence of glaucoma appearing at ages varying between 10 and 40 years.

Related symptoms:

  • Seizures
  • Short stature
  • Generalized hypotonia
  • Pain
  • Feeding difficulties


SOURCES: ORPHANET MENDELIAN

More info about CATARACT-GLAUCOMA SYNDROME

Medium match DIFFUSE CUTANEOUS SYSTEMIC SCLEROSIS


Diffuse cutaneous systemic sclerosis (dcSSc) is a subtype of Systemic Sclerosis (SSc; see this term) characterized by truncal and acral skin fibrosis with an early and significant incidence of diffuse involvement (interstitial lung disease, oliguric renal failure, diffuse gastrointestinal disease, and myocardial involvement).

DIFFUSE CUTANEOUS SYSTEMIC SCLEROSIS Is also known as progressive cutaneous systemic scleroderma|diffuse cutaneous systemic scleroderma|progressive cutaneous systemic sclerosis

Related symptoms:

  • Muscle weakness
  • Pain
  • Flexion contracture
  • Hypertension
  • Dysphagia


SOURCES: ORPHANET MENDELIAN

More info about DIFFUSE CUTANEOUS SYSTEMIC SCLEROSIS

Low match FAMILIAL MEDITERRANEAN FEVER


Familial Mediterranean fever (FMF) is an autoinflammatory disorder characterized by recurrent short episodes of fever and serositis resulting in pain in the abdomen, chest, joints and muscles.

FAMILIAL MEDITERRANEAN FEVER Is also known as benign paroxysmal peritonitis|familial paroxysmal polyserositis|benign recurrent polyserositis|polyserositis, familial paroxysmal|fmf|periodic disease|familial mediterranean fever, autosomal recessive|polyserositis, recurrent

Related symptoms:

  • Seizures
  • Pain
  • Anemia
  • Hepatomegaly
  • Fever


SOURCES: OMIM ORPHANET MENDELIAN

More info about FAMILIAL MEDITERRANEAN FEVER

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Other less relevant matches:

Low match ATTRV30M AMYLOIDOSIS


Familial amyloid polyneuropathy (FAP) or transthyretin (TTR) amyloid polyneuropathy is a progressive sensorimotor and autonomic neuropathy of adulthood onset. Weight loss and cardiac involvement are frequent; ocular or renal complications may also occur.

ATTRV30M AMYLOIDOSIS Is also known as familial amyloid polyneuropathy type i|ttr amyloid neuropathy|attrv30m-related amyloidosis|hereditary amyloidosis, transthyretin-related|transthyretin amyloid polyneuropathy|familial amyloid polyneuropathy, portuguese-swedish-japanese type|fap|amyloid pol

Related symptoms:

  • Seizures
  • Hearing impairment
  • Ataxia
  • Nystagmus
  • Sensorineural hearing impairment


SOURCES: OMIM ORPHANET MENDELIAN

More info about ATTRV30M AMYLOIDOSIS

Low match CRANIO-OSTEOARTHROPATHY


Cranio-osteoarthropathy (COA) is a form of primary hypertrophic osteoarthropathy (see this term) characterized by delayed closure of the cranial sutures and fontanels, digital clubbing, arthropathy, and periostosis.

CRANIO-OSTEOARTHROPATHY Is also known as sdam|currarino idiopathic osteoarthropathy|currarino disease|reginato-schiapachasse syndrome

Related symptoms:

  • Ventricular septal defect
  • Headache
  • Patent ductus arteriosus
  • Constipation
  • Diabetes mellitus


SOURCES: ORPHANET OMIM MENDELIAN

More info about CRANIO-OSTEOARTHROPATHY

Low match TUMOR NECROSIS FACTOR RECEPTOR 1 ASSOCIATED PERIODIC SYNDROME


Tumor necrosis factor receptor 1 associated periodic syndrome (TRAPS) is a periodic fever syndrome, characterized by recurrent fever, arthralgia, myalgia and tender skin lesions lasting for 1 to 3 weeks, associated with skin, joint, ocular and serosal inflammation and complicated by secondary amyloidosis (see this term).

TUMOR NECROSIS FACTOR RECEPTOR 1 ASSOCIATED PERIODIC SYNDROME Is also known as tnf receptor 1-associated periodic syndrome|fpf|traps syndrome|hibernian fever, familial|familial hibernian fever|fhf|tnf receptor-associated periodic syndrome|tumor necrosis factor receptor-associated periodic syndrome|traps

Related symptoms:

  • Neoplasm
  • Pain
  • Anemia
  • Fever
  • Edema


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about TUMOR NECROSIS FACTOR RECEPTOR 1 ASSOCIATED PERIODIC SYNDROME

Low match EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE


Ehlers-Danlos syndrome, hypermobility type (HT-EDS) is the most frequent form of EDS (see this term), a group of hereditary connective tissue diseases, and is characterized by joint hyperlaxity, mild skin hyperextensibility, tissue fragility and extra-musculoskeletal manifestations.

EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE Is also known as benign joint hypermobility syndrome|ehlers-danlos syndrome, hypermobile type|ht-eds|ehlers-danlos syndrome, type iii|benign hypermobility syndrome|ehlers-danlos syndrome type 3|eds iii|eds3|bjhs

Related symptoms:

  • Scoliosis
  • Pain
  • Ptosis
  • Epicanthus
  • Fatigue


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about EHLERS-DANLOS SYNDROME, HYPERMOBILITY TYPE

Low match HYPERIMMUNOGLOBULINEMIA D WITH PERIODIC FEVER


Hyperimmunoglobinemia D with periodic fever (HIDS) is a rare autoinflammatory disease characterized by periodic attacks of fever and a systemic inflammatory reaction (cervical lymphadenopathy, abdominal pain, vomiting, diarrhea, arthralgias and skin signs).

HYPERIMMUNOGLOBULINEMIA D WITH PERIODIC FEVER Is also known as hyperimmunoglobinemia d with recurrent fever|hyper-igd syndrome|hyperimmunoglobulinemia d and periodic fever syndrome|partial mevalonate kinase deficiency|hids|periodic fever, dutch type|hyperimmunoglobulinemia d syndrome

Related symptoms:

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


SOURCES: OMIM ORPHANET MENDELIAN

More info about HYPERIMMUNOGLOBULINEMIA D WITH PERIODIC FEVER

Low match FLOATING-HARBOR SYNDROME


Floating-Harbor syndrome is a genetic developmental disorder characterized by facial dysmorphism, short stature with delayed bone age, and expressive language delay.

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Hearing impairment


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about FLOATING-HARBOR SYNDROME

Low match 22Q11.2 DELETION SYNDROME


22q11.2 deletion syndrome (DS) is a chromosomal anomaly which causes a congenital malformation disorder whose common features include cardiac defects, palatal anomalies, facial dysmorphism, developmental delay and immune deficiency.

22Q11.2 DELETION SYNDROME Is also known as monosomy 22q11|digeorge sequence|sedlackova syndrome|takao syndrome|velocardiofacial syndrome|shprintzen syndrome|conotruncal anomaly face syndrome|digeorge syndrome|catch 22|cayler cardiofacial syndrome|microdeletion 22q11.2|22q11ds

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Hearing impairment


SOURCES: ORPHANET MENDELIAN

More info about 22Q11.2 DELETION SYNDROME

Top 5 symptoms//phenotypes associated to Arthritis and Constipation

Symptoms // Phenotype % cases
Vomiting Common - Between 50% and 80% cases
Arthralgia Common - Between 50% and 80% cases
Pain Common - Between 50% and 80% cases
Headache Common - Between 50% and 80% cases
Seizures Common - Between 50% and 80% cases
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Other less frequent symptoms

Patients with Arthritis and Constipation. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Diarrhea Malabsorption Myalgia Fever Inguinal hernia Gastroesophageal reflux Amyloidosis Vasculitis Migraine Nausea Renal insufficiency Splenomegaly Abnormality of the dentition Skin rash Erysipelas Vertigo Meningitis Arrhythmia Scoliosis Purpura Depressivity Nausea and vomiting Abdominal pain Lymphadenopathy Umbilical hernia Short stature Osteoarthritis Intestinal obstruction Erythema Paresthesia Hearing impairment Hypertension Peritonitis Microcephaly Global developmental delay Intellectual disability Neoplasm Episodic fever Joint hyperflexibility Leukocytosis Elevated erythrocyte sedimentation rate

Rare Symptoms - Less than 30% cases


Short philtrum Orchitis Anal atresia Ataxia Dysarthria Patent ductus arteriosus Telecanthus Eczema Feeding difficulties in infancy Prominent nasal bridge Nasal speech Hydrocephalus Bulbous nose Meningocele Joint stiffness Ventricular septal defect Urinary incontinence Peripheral demyelination Syringomyelia Lipoma Urinary retention Spina bifida Abnormality of the skull Hypothyroidism Behavioral abnormality Micrognathia Limitation of joint mobility Microdontia Wide nasal bridge Low-set ears Cryptorchidism Abnormal facial shape Strabismus Acrocyanosis Intrauterine growth retardation Anorectal anomaly Long eyelashes Growth delay Hypertelorism Failure to thrive Cataract Gastrointestinal hemorrhage Abdominal distention Short neck Anxiety Neuritis Papule Conductive hearing impairment Conjunctivitis Hypermelanotic macule Uveitis Upslanted palpebral fissure Chills Optic neuritis Atrial septal defect Hypospadias Abnormality of cardiovascular system morphology Ptosis Epicanthus Fatigue Dilatation Intellectual disability, mild Joint laxity Serositis Postnatal growth retardation Carious teeth Craniosynostosis Autoimmunity Nephrocalcinosis Rheumatoid arthritis Nephrotic syndrome Hypertensive crisis Osteolysis Pericarditis Anemia Muscle weakness Hepatosplenomegaly Hepatomegaly Stiff neck Congestive heart failure Asthma Pneumonia Chest pain Generalized hypotonia Weight loss Flexion contracture Nephropathy Pleuritis Turricephaly Abnormal heart morphology Clinodactyly Hypoparathyroidism Varicose veins Patellar dislocation Multiple renal cysts Truncus arteriosus Atelectasis Abnormal eyelid morphology Abnormal lung lobation Bipolar affective disorder Attention deficit hyperactivity disorder Delayed skeletal maturation Dysphasia Wide mouth Intellectual disability, moderate Abnormality of the thorax Overfolded helix Aggressive behavior Chronic otitis media Acne Hydronephrosis Deeply set eye Clinodactyly of the 5th finger Bowel incontinence Thin upper lip vermilion Kyphoscoliosis Mandibular prognathia Foot polydactyly Hyperactivity Posterior embryotoxon Posteriorly rotated ears Babinski sign Hyperthyroidism Abnormality of the skeletal system Chronic obstructive pulmonary disease Optic disc pallor Poor coordination Peripheral visual field loss Subcapsular cataract Colitis Apathy Urticaria Impaired T cell function Recurrent pneumonia Abnormal pulmonary valve morphology Dehydration Large forehead Aciduria Retinal arteriolar tortuosity Abnormal aortic arch morphology Multiple suture craniosynostosis Tricuspid atresia Abnormality of the tonsils Sepsis Retinal dystrophy Infertility Posterior subcapsular cataract Arrhinencephaly Abnormality of the uterus Cognitive impairment Gait disturbance Corneal neovascularization Tetany Hypoplasia of the thymus Seborrheic dermatitis Brachydactyly Hyperreflexia Delayed speech and language development High palate Abnormal thrombocyte morphology Recurrent aphthous stomatitis Abnormal aortic valve morphology Abnormality of the pharynx Small earlobe Platybasia Pharyngitis Cervical lymphadenopathy Neutrophilia Porokeratosis Increased IgA level Camptodactyly of finger Hypermetropia Hand polydactyly Expressive language delay Curved fingers Enlarged naris Choanal atresia Epididymal cyst Congenital posterior urethral valve Congenital pseudoarthrosis of the clavicle Pseudoarthrosis Persistent left superior vena cava Varicocele Short upper lip Tetralogy of Fallot Spinal dysraphism Tethered cord Broad columella Hyperextensibility of the finger joints Speech apraxia Enlarged joints Cough Villous atrophy Aganglionic megacolon Enuresis Renal hypoplasia Broad fingertip Abnormality of the clavicle Vesicoureteral reflux Narrow mouth Arachnodactyly Autism Long face Glaucoma Obesity Thrombocytopenia Microphthalmia Immunodeficiency Malar flattening Abnormal soft palate morphology Intestinal malrotation Long philtrum Talipes equinovarus Downslanted palpebral fissures Optic atrophy Cleft palate Muscular hypotonia Specific learning disability Mesocardia Generalized cerebral atrophy/hypoplasia Short attention span Short columella Neurological speech impairment Prominent nose Low posterior hairline Interphalangeal joint contracture of finger Cholelithiasis Apraxia Coarctation of aorta Hypoplasia of penis Otitis media Underdeveloped nasal alae Dental malocclusion Broad nasal tip Recurrent otitis media Triangular face Hypoplasia of the maxilla Small hand Downturned corners of mouth Hirsutism Thin vermilion border Smooth philtrum Poor speech Polyhydramnios Small for gestational age Short palpebral fissure Broad thumb Cone-shaped epiphyses of the phalanges of the hand Abnormality of dental enamel Sprengel anomaly Short clavicles Proportionate short stature Hypocalcemia Celiac disease High pitched voice Preauricular pit Impulsivity Clubbing Language impairment Short thumb Hypopigmented skin patches Trigonocephaly Schizophrenia Abnormality of the voice Laryngomalacia Abnormality of the hand Polycystic kidney dysplasia Abnormality of the fingernails Finger clinodactyly Generalized hirsutism 11 pairs of ribs Pes planus Nyctalopia Tremor Gliosis Coma Polyneuropathy Peripheral axonal neuropathy Paraplegia Facial palsy Dementia Hyporeflexia Areflexia Cardiomyopathy Peripheral neuropathy Neuronal loss in central nervous system Visual impairment Spasticity Sensorineural hearing impairment Nystagmus Recurrent meningitis Azotemia Renal amyloidosis Gastrointestinal infarctions Congenital hypoplastic anemia Synovitis Hypotension Bilateral sensorineural hearing impairment Anemia of inadequate production Axonal degeneration Sensory ataxia Abnormal renal physiology Myelopathy Constrictive median neuropathy Stroke-like episode Multiple myeloma Restrictive cardiomyopathy Increased CSF protein Decreased number of peripheral myelinated nerve fibers Orthostatic hypotension Aphasia Cardiomegaly Malnutrition Impotence Cerebral hemorrhage Cachexia Atrioventricular block Spastic paraparesis Paraparesis Abnormal autonomic nervous system physiology Hallucinations Hemiparesis Decreased circulating aldosterone level Oral leukoplakia Orthostatic hypotension due to autonomic dysfunction Premature loss of teeth Telangiectasia Pulmonary arterial hypertension Abnormality of the skin Dyspnea Dysphagia Pulmonary insufficiency Premature loss of primary teeth Chronic pain Chondrocalcinosis Papilledema Osteomalacia Pulmonary fibrosis Rickets Hypercalcemia Increased intracranial pressure Bone pain Waddling gait Proptosis Respiratory failure Brachycephaly Respiratory distress Feeding difficulties Skin ulcer Telangiectasia of the skin Acute hepatic failure Ascites Edema of the lower limbs Antinuclear antibody positivity Gout Increased serum ferritin Hyperkalemia Inflammation of the large intestine Systemic lupus erythematosus Chronic kidney disease Pancreatitis Myocardial infarction Stage 5 chronic kidney disease Scleroderma Abnormality of the kidney Proteinuria Acidosis Abnormal bowel sounds Narrow foramen obturatorium Decreased urine output Dyspareunia Oliguria Osteolytic defects of the phalanges of the hand Pulmonary infiltrates Xerostomia Psychomotor deterioration Vitreous floaters Pallor Abnormality of the foot Decreased nerve conduction velocity Abnormal palate morphology Joint dislocation Wormian bones Gingival overgrowth Subcutaneous nodule Thin skin Mitral valve prolapse Sleep disturbance Joint hypermobility Hip dislocation Elbow dislocation Apnea Osteoporosis Fasciitis Hepatic amyloidosis Abnormality of the sacroiliac joint Conjunctival hyperemia Lymphocytosis Periorbital edema Elevated C-reactive protein level Recurrent pharyngitis Hyperextensible skin Decreased fertility Myositis Abnormality of the menstrual cycle Hyperhidrosis Rod-cone dystrophy Blindness Frontal bossing Genital hernia Cystocele Tendon rupture Premature rupture of membranes Arterial dissection Abnormality of the gingiva Ascending tubular aorta aneurysm Keratoconus Venous insufficiency Gastrointestinal dysmotility Aplasia/Hypoplasia of the abdominal wall musculature Abnormality of the wrist Atypical scarring of skin Gingivitis Soft skin Aortic root aneurysm Striae distensae Keratoconjunctivitis sicca Abnormal myocardium morphology Reticulocytosis Cardiac amyloidosis Tracheoesophageal fistula Deviation of finger Abnormality of the knee Neurogenic bladder Abnormal cortical bone morphology Abnormality of tibia morphology Chronic constipation Maternal diabetes Joint swelling Transposition of the great arteries Hyperostosis Back pain Bladder exstrophy Abnormality of the genitourinary system Holoprosencephaly Spina bifida occulta Type I diabetes mellitus Situs inversus totalis Large fontanelles Omphalocele Talipes Diabetes mellitus Amyloid deposition in the vitreous humor Teratoma Spinal deformities Cellulitis Hemisacrum Macule Cranial nerve paralysis Muscle stiffness Bruising susceptibility Hepatic failure Hernia Edema Hydromyelia Presacral teratoma Anterior sacral meningocele Cloacal exstrophy Lower limb undergrowth Rectal fistula Sacral meningocele Sacral lipoma Sirenomelia Dermoid cyst Exstrophy Rectal abscess Absence of the sacrum Clubbing of toes Cyclopia Mottled pigmentation Occipital myelomeningocele



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