Congestive heart failure, and Inflammation of the large intestine

Diseases related with Congestive heart failure and Inflammation of the large intestine

In the following list you will find some of the most common rare diseases related to Congestive heart failure and Inflammation of the large intestine that can help you solving undiagnosed cases.


Top matches:

Medium match COMBINED IMMUNODEFICIENCY DUE TO LRBA DEFICIENCY


Common variable immunodeficiency-8 with autoimmunity is an autosomal recessive disorder of immune dysregulation. Affected individuals have early childhood onset of recurrent infections, particularly respiratory infections, and also develop variable autoimmune disorders, including idiopathic thrombocytopenic purpura, autoimmune hemolytic anemia, and inflammatory bowel disease. The presentation and phenotype are highly variable, even within families (summary by Lopez-Herrera et al., 2012 and Alangari et al., 2012). Immunologic findings are also variable and may include decreased B cells, hypogammaglobulinemia, and deficiency of CD4+ T regulatory (Treg) cells (Charbonnier et al., 2015).For a general description and a discussion of genetic heterogeneity of common variable immunodeficiency, see CVID1 (OMIM ).

COMBINED IMMUNODEFICIENCY DUE TO LRBA DEFICIENCY Is also known as cid due to lrba deficiency

Related symptoms:

  • Growth delay
  • Neoplasm
  • Failure to thrive
  • Anemia
  • Diarrhea


SOURCES: OMIM ORPHANET MENDELIAN

More info about COMBINED IMMUNODEFICIENCY DUE TO LRBA DEFICIENCY

Medium match PRIMARY SCLEROSING CHOLANGITIS


Primary sclerosing cholangitis (PSC) is a rare, slowly progressive liver disease characterized by inflammation and destruction of the intra- and/or extra-hepatic bile ducts that lead to cholestasis, liver fibrosis, liver cirrhosis and ultimately liver failure.

PRIMARY SCLEROSING CHOLANGITIS Is also known as psc

Related symptoms:

  • Pain
  • Hypertension
  • Hepatomegaly
  • Fever
  • Fatigue


SOURCES: ORPHANET OMIM MENDELIAN

More info about PRIMARY SCLEROSING CHOLANGITIS

Medium match AUTOIMMUNE ENTEROPATHY AND ENDOCRINOPATHY-SUSCEPTIBILITY TO CHRONIC INFECTIONS SYNDROME


Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome is an extremely rare, autosomal dominant immunological disorder characterized by variable enteropathy, endocrine disorders (e.g. type 1 diabetes mellitus, hypothyroidism), immune dysregulation with pulmonary and blood-borne bacterial infections, and fungal infections (chronic mucocutaneous candidiasis) developing in infancy. Other manifestations include short stature, eczema, hepatosplenomegaly, delayed puberty, and osteoporosis/osteopenia.

AUTOIMMUNE ENTEROPATHY AND ENDOCRINOPATHY-SUSCEPTIBILITY TO CHRONIC INFECTIONS SYNDROME Is also known as candf7|candidiasis, familial, 7|candidiasis, familial chronic mucocutaneous, autosomal dominant

Related symptoms:

  • Global developmental delay
  • Short stature
  • Growth delay
  • Anemia
  • Diarrhea


SOURCES: ORPHANET OMIM MENDELIAN

More info about AUTOIMMUNE ENTEROPATHY AND ENDOCRINOPATHY-SUSCEPTIBILITY TO CHRONIC INFECTIONS SYNDROME

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Other less relevant matches:

Low match D-BIFUNCTIONAL PROTEIN DEFICIENCY


D-bifunctional protein deficiency is a disorder of peroxisomal fatty acid beta-oxidation. See also peroxisomal acyl-CoA oxidase deficiency (OMIM ), caused by mutation in the ACOX1 gene (OMIM ) on chromosome 17q25. The clinical manifestations of these 2 deficiencies are similar to those of disorders of peroxisomal assembly, including X-linked adrenoleukodystrophy (ALD ), Zellweger cerebrohepatorenal syndrome (see {214100}) and neonatal adrenoleukodystrophy (NALD; see {601539}) (Watkins et al., 1995).DBP deficiency has been classified into 3 subtypes depending upon the deficient enzyme activity. Type I is a deficiency of both 2-enoyl-CoA hydratase and 3-hydroxyacyl-CoA dehydrogenase; type II is a deficiency of hydratase activity alone; and type III is a deficiency of dehydrogenase activity alone. Virtually all patients with types I, II, and III have a severe phenotype characterized by infantile-onset of hypotonia, seizures, and abnormal facial features, and most die before age 2 years. McMillan et al. (2012) proposed a type IV deficiency on the basis of less severe features; these patients have a phenotype reminiscent of Perrault syndrome (PRLTS1 ). Pierce et al. (2010) noted that Perrault syndrome and DBP deficiency overlap clinically and suggested that DBP deficiency may be underdiagnosed.

D-BIFUNCTIONAL PROTEIN DEFICIENCY Is also known as peroxisomal bifunctional enzyme deficiency|dbp deficiency|17-beta-hydroxysteroid dehydrogenase iv deficiency|pbfe deficiency

Related symptoms:

  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Hearing impairment
  • Hypertelorism


SOURCES: ORPHANET OMIM MENDELIAN

More info about D-BIFUNCTIONAL PROTEIN DEFICIENCY

Low match SARCOIDOSIS


Sarcoidosis is a multisystemic disorder of unknown cause characterized by the formation of immune granulomas in involved organs.

SARCOIDOSIS Is also known as boeck sarcoid|besnier-boeck-schaumann disease|sarcoidosis|boeck's sarcoid

Related symptoms:

  • Seizures
  • Pain
  • Cataract
  • Anemia
  • Visual impairment


SOURCES: ORPHANET OMIM MENDELIAN

More info about SARCOIDOSIS

Low match POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1


Polyglucosan body myopathy-1 is an autosomal recessive disorder characterized by onset in childhood of progressive proximal muscle weakness, resulting in difficulties in ambulation. Most patients also develop progressive dilated cardiomyopathy, which may necessitate cardiac transplant in severe cases. A small subset of patients present with severe immunodeficiency and a hyperinflammatory state in very early childhood (summary by Boisson et al., 2012 and Nilsson et al., 2013). Genetic Heterogeneity of Polyglucosan Body MyopathySee also PGBM2 (OMIM ), caused by mutation in the GYG1 gene (OMIM ) on chromosome 3q24.

POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1 Is also known as polyglucosan body myopathy, early-onset, with or without immunodeficiency|pbmei

Related symptoms:

  • Scoliosis
  • Growth delay
  • Failure to thrive
  • Muscle weakness
  • Ptosis


SOURCES: OMIM MENDELIAN

More info about POLYGLUCOSAN BODY MYOPATHY 1 WITH OR WITHOUT IMMUNODEFICIENCY; PGBM1

Low match PRADER-WILLI SYNDROME; PWS


Prader-Willi syndrome is characterized by diminished fetal activity, obesity, muscular hypotonia, mental retardation, short stature, hypogonadotropic hypogonadism, and small hands and feet. It can be considered to be an autosomal dominant disorder and is caused by deletion or disruption of a gene or several genes on the proximal long arm of the paternal chromosome 15 or maternal uniparental disomy 15, because the gene(s) on the maternal chromosome(s) 15 are virtually inactive through imprinting. Horsthemke and Wagstaff (2008) provided a detailed review of the mechanisms of imprinting of the Prader-Willi/Angelman syndrome (OMIM ) region.See also the chromosome 15q11-q13 duplication syndrome (OMIM ), which shows overlapping clinical features.

PRADER-WILLI SYNDROME; PWS Is also known as prader-labhart-willi syndrome

Related symptoms:

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


SOURCES: OMIM MENDELIAN

More info about PRADER-WILLI SYNDROME; PWS

Low match LONG CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY


Long chain 3-hydroxyacyl-CoA dehydrogenase deficiency (LCHADD) is a mitochondrial disorder of long chain fatty acid oxidation characterized in most patients by onset in infancy/ early childhood with hypoketotic hypoglycemia, metabolic acidosis, liver disease, hypotonia and frequently cardiac involvement with arrhythmias and/or cardiomyopathy.

LONG CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY Is also known as lchad deficiency|long-chain 3-hydroxyacyl-coenzyme a dehydrogenase deficiency|lchadd

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Failure to thrive


SOURCES: ORPHANET OMIM MENDELIAN

More info about LONG CHAIN 3-HYDROXYACYL-COA DEHYDROGENASE DEFICIENCY

Low match ARTERIAL TORTUOSITY SYNDROME


Arterial tortuosity syndrome (ATS) is a rare connective tissue disorder characterized by tortuosity and elongation of the large and medium-sized arteries and a propensity towards aneurysm formation, vascular dissection, and stenosis of the pulmonary arteries.

ARTERIAL TORTUOSITY SYNDROME Is also known as ats

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Scoliosis
  • Hypertelorism
  • Strabismus


SOURCES: ORPHANET MENDELIAN

More info about ARTERIAL TORTUOSITY SYNDROME

Low match MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY; MADD


Glutaric aciduria II (GA2) is an autosomal recessively inherited disorder of fatty acid, amino acid, and choline metabolism. It differs from GA I (GA1 ) in that multiple acyl-CoA dehydrogenase deficiencies result in large excretion not only of glutaric acid, but also of lactic, ethylmalonic, butyric, isobutyric, 2-methyl-butyric, and isovaleric acids. GA II results from deficiency of any 1 of 3 molecules: the alpha (ETFA) and beta (ETFB) subunits of electron transfer flavoprotein, and electron transfer flavoprotein dehydrogenase (ETFDH). The clinical picture of GA II due to the different defects appears to be indistinguishable; each defect can lead to a range of mild or severe cases, depending presumably on the location and nature of the intragenic lesion, i.e., mutation, in each case (Goodman, 1993; Olsen et al., 2003).The heterogeneous clinical features of patients with MADD fall into 3 classes: a neonatal-onset form with congenital anomalies (type I), a neonatal-onset form without congenital anomalies (type II), and a late-onset form (type III). The neonatal-onset forms are usually fatal and are characterized by severe nonketotic hypoglycemia, metabolic acidosis, multisystem involvement, and excretion of large amounts of fatty acid- and amino acid-derived metabolites. Symptoms and age at presentation of late-onset MADD are highly variable and characterized by recurrent episodes of lethargy, vomiting, hypoglycemia, metabolic acidosis, and hepatomegaly often preceded by metabolic stress. Muscle involvement in the form of pain, weakness, and lipid storage myopathy also occurs. The organic aciduria in patients with the late-onset form of MADD is often intermittent and only evident during periods of illness or catabolic stress (summary by Frerman and Goodman, 2001).Importantly, riboflavin treatment has been shown to ameliorate the symptoms and metabolic profiles in many MADD patients, particularly those with type III, the late-onset and mildest form (Liang et al., 2009).

MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY; MADD Is also known as ema|ethylmalonic-adipicaciduria|glutaric aciduria ii|ga ii|glutaric acidemia ii|ga2

Related symptoms:

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


SOURCES: OMIM ORPHANET MENDELIAN

More info about MULTIPLE ACYL-COA DEHYDROGENASE DEFICIENCY; MADD

Top 5 symptoms//phenotypes associated to Congestive heart failure and Inflammation of the large intestine

Symptoms // Phenotype % cases
Hepatomegaly Common - Between 50% and 80% cases
Failure to thrive Common - Between 50% and 80% cases
Global developmental delay Common - Between 50% and 80% cases
Elevated hepatic transaminase Uncommon - Between 30% and 50% cases
Seizures Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Congestive heart failure and Inflammation of the large intestine. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Abnormality of the liver Pain Weight loss Fatigue Fever Growth delay Hypertension Myopathy Muscular hypotonia Intellectual disability Dilated cardiomyopathy Type I diabetes mellitus Osteopenia Dilatation Generalized hypotonia Hepatosplenomegaly Respiratory failure Macrocephaly Strabismus Jaundice Abnormal facial shape Hypertrophic cardiomyopathy Immune dysregulation Decreased liver function Depressed nasal bridge Cataract Anorexia Edema Hepatic steatosis Respiratory distress Proximal muscle weakness Photophobia Dyspnea Scoliosis Hypopigmentation of the skin Cardiomyopathy Feeding difficulties Hypothyroidism Respiratory tract infection Autoimmunity Lymphadenopathy Hemolytic anemia Recurrent respiratory infections Pneumonia Hypoglycemia Vomiting Myopia Recurrent infections Immunodeficiency Bronchiectasis Thrombocytopenia Gastrointestinal inflammation Diarrhea Elevated serum creatine phosphokinase Anemia Diabetes mellitus Splenomegaly

Rare Symptoms - Less than 30% cases


Hypertelorism Abnormality of the cerebral white matter Dolichocephaly Neonatal hypotonia High forehead Upslanted palpebral fissure Visual loss Nystagmus Ventriculomegaly Talipes equinovarus Delayed skeletal maturation Renal cyst Delayed puberty Micrognathia Eczema Skeletal muscle atrophy Epicanthus Pulmonary embolism Enterocolitis Visual impairment High palate Sepsis Cardiac arrest Gliosis Motor delay Neoplasm Myalgia Nausea Metabolic acidosis Coma Hypothermia Rhabdomyolysis Chorioretinal atrophy Hypoketotic hypoglycemia Progressive proximal muscle weakness Elevated plasma acylcarnitine levels Reye syndrome-like episodes Hepatic failure Behavioral abnormality Peripheral demyelination Short nose Joint hyperflexibility Abnormality of the pinna Arachnodactyly Arrhythmia Specific learning disability Headache Hip dysplasia Peripheral neuropathy Muscle weakness Cardiorespiratory arrest Decreased muscle mass Pachygyria Heterotopia Short stature Polymicrogyria Cor pulmonale Villous atrophy Scarring Abdominal pain Pancytopenia Autoimmune thrombocytopenia Osteoporosis Encephalopathy Depressivity Renal insufficiency Purpura Inflammatory abnormality of the skin Cholestasis Interstitial pulmonary abnormality Uveitis Ascites Thyroiditis Pruritus Autoimmune hemolytic anemia Hepatitis Generalized lymphadenopathy Abnormal lung morphology Cholestatic liver disease Abnormal intestine morphology Fatigable weakness Pleural effusion Pancreatitis Arthritis Portal hypertension Recurrent upper respiratory tract infections Temperature instability Central adrenal insufficiency Hypoplastic labia minora Erysipelas Triangular mouth Disseminated intravascular coagulation Frontal upsweep of hair Clitoral hypoplasia Anteverted ears Poor fine motor coordination Abdominal obesity Generalized hypopigmentation Ocular albinism Chromosome breakage Hypoplasia of the fovea Psychotic episodes Abnormality of metabolism/homeostasis Narrow palm Pigmentary retinopathy Recurrent hypoglycemia Preeclampsia Impaired mastication Limb tremor Multiple lipomas Loss of consciousness Abnormal electroretinogram Tachypnea Hypocalcemia Sensorimotor neuropathy Abnormality of retinal pigmentation Exotropia Brain atrophy Hypopnea Renal cortical cysts Polyneuropathy Cataplexy Retinal dystrophy Narcolepsy Peripheral axonal neuropathy Nyctalopia Retinopathy Oligomenorrhea Acromicria Poor gross motor coordination Almond-shaped palpebral fissure Acrocyanosis Ragged-red muscle fibers Overweight Insulin resistance Poor suck Infantile muscular hypotonia Scrotal hypoplasia Sleep apnea Bicuspid aortic valve Narrow palpebral fissure Spontaneous abortion Hypogonadotrophic hypogonadism Increased body weight Aortic valve stenosis Abnormality of branched chain family amino acid metabolism Bradycardia Defective dehydrogenation of isovaleryl CoA and butyryl CoA Fatigable weakness of neck muscles Clumsiness Primary amenorrhea Cutaneous photosensitivity Psychosis Type II diabetes mellitus Decreased fetal movement Oligohydramnios Hepatic periportal necrosis Narrow forehead Abnormality of the cardiovascular system Amenorrhea Electron transfer flavoprotein-ubiquinone oxidoreductase defect Febrile seizures Nasal speech Failure to thrive in infancy Central hypotonia Narrow nasal bridge Abnormality of lipid metabolism Iris hypopigmentation Reduced consciousness/confusion Hypopigmentation of hair Striae distensae Arthralgia of the hip Glutaric acidemia Impaired pain sensation Increased muscle lipid content Ketotic hypoglycemia Reduced protein C activity Myeloid leukemia Polyphagia Precocious puberty External genital hypoplasia Truncal obesity Adrenal insufficiency Skeletal muscle hypertrophy Ethylmalonic aciduria Albinism Glucose intolerance Hypersarcosinemia Large hands Fatigable weakness of distal limb muscles Emotional lability Radial deviation of finger Hyperinsulinemia Hypoventilation Decreased activity of 3-hydroxyacyl-CoA dehydrogenase Decreased plasma carnitine Ketonuria Telecanthus Stridor Ventricular fibrillation Difficulty walking Restrictive ventilatory defect Difficulty climbing stairs Glycosuria Acute kidney injury Drowsiness Myoglobinuria Arthralgia Ketosis Excessive daytime somnolence Lethargy Chronic fatigue Organic aciduria Acidosis Gait ataxia Exercise-induced myalgia Medulloblastoma Areflexia Respiratory insufficiency Dysphagia Gait disturbance Tremor Proximal tubulopathy Hyperlordosis Congenital cataract Spasticity Left ventricular hypertrophy Poor head control Hyperammonemia Easy fatigability Slurred speech Polycystic kidney dysplasia Spastic tetraparesis Scapular winging Exercise intolerance Clonus Leukodystrophy Back pain Wide anterior fontanel Renal dysplasia Nausea and vomiting Abnormality of the genital system Tetraparesis Hemiplegia Cardiomegaly Waddling gait Aciduria Increased serum lactate Generalized muscle weakness Tetraplegia Muscle cramps Pulmonary hypoplasia Lactic acidosis Limb muscle weakness Dysarthria Episodic vomiting Abnormal left ventricle morphology Macrotia Coxa valga Thin skin Oliguria Myocardial infarction Short palpebral fissure Long face Hip dislocation Blepharophimosis Craniosynostosis Glutaric aciduria Progressive spastic quadriplegia Gastroesophageal reflux Clinodactyly of the 5th finger Hyperextensible skin Inguinal hernia Malar flattening 3-hydroxydicarboxylic aciduria Abnormality of acid-base homeostasis Personality disorder Mutism Posterior staphyloma Hypoglycemic coma Acute hepatic steatosis Nonketotic hypoglycemia Abnormal chorioretinal morphology Hepatic encephalopathy Coxa vara Redundant skin Ataxia Arterial stenosis Abnormality of the zygomatic bone Abnormality of the renal tubule Abnormal corpus callosum morphology Abnormal carotid artery morphology Esotropia Loss of ability to walk Keratoglobus Long palm Acute pancreatitis Median cleft lip and palate Respiratory arrest Femoral hernia Avascular necrosis of the capital femoral epiphysis Pyloric stenosis Abnormal myocardium morphology Myocarditis Esophagitis Generalized aminoaciduria Aortic dissection Hiatus hernia Pulmonary artery stenosis Aortic root aneurysm Prematurely aged appearance Keratoconus Telangiectasia of the skin Rocker bottom foot Aortic aneurysm Growth hormone deficiency Maculopapular exanthema Gastrointestinal hemorrhage Carotid artery dilatation Cerebellar atrophy Hypoplasia of the corpus callosum Frontal bossing Optic atrophy Low-set ears Hearing impairment Abnormal serum interferon-gamma level Medial calcification of large arteries Esophageal carcinoma Oropharyngeal squamous cell carcinoma Susceptibility to herpesvirus Recurrent Aspergillus infections Functional abnormality of the bladder Hypospadias Autoimmune neutropenia Renal artery stenosis Renovascular hypertension Antiphospholipid antibody positivity B lymphocytopenia Primary hypothyroidism Decrease in T cell count Generalized osteoporosis Chronic mucocutaneous candidiasis Abnormality of the endocrine system Dilatation of the cerebral artery Hashimoto thyroiditis Long philtrum Pectus excavatum Encephalitis Thoracic hypoplasia Renal cortical microcysts Chylous ascites Cerebral hypoplasia Cerebral dysmyelination Bile duct proliferation Corpus callosum atrophy Undetectable electroretinogram Aspiration pneumonia Adrenal hypoplasia Scaphocephaly Primary adrenal insufficiency Cortical dysplasia Delayed cranial suture closure Polyhydramnios Aplasia/Hypoplasia of the cerebellum Hammertoe Decreased nerve conduction velocity Progressive hearing impairment Aspiration Large fontanelles Split hand Progressive visual loss Abdominal distention Talipes Severe global developmental delay Feeding difficulties in infancy Retrognathia Patent foramen ovale Leukoencephalopathy Calcific stippling Exocrine pancreatic insufficiency Hypoalbuminemia Hepatic fibrosis Cirrhosis Burkitt lymphoma Follicular hyperplasia Interstitial pneumonitis Gastritis IgM deficiency Verrucae Brain neoplasm Clubbing of fingers Chronic lung disease IgA deficiency Generalized amyotrophy Recurrent sinusitis Colitis Combined immunodeficiency Clubbing Conjunctivitis Chronic diarrhea Recurrent otitis media Otitis media Decreased antibody level in blood Lymphoma Asthma Neutropenia Cholelithiasis Abnormality of the thyroid gland Lymphopenia Chronic hepatic failure Pulmonary arterial hypertension Carcinoma Adenocarcinoma of the large intestine Dilated superficial abdominal veins Recurrent systemic pyogenic infections Neoplasm of the gallbladder Abnormal large intestine physiology Spider hemangioma Polyclonal elevation of IgM Elevated alkaline phosphatase of hepatic origin Palmar telangiectasia Abnormal biliary tract morphology Vitamin K deficiency Celiac disease Vitamin A deficiency Cholangiocarcinoma Vitamin E deficiency Sclerosing cholangitis Abnormal eosinophil morphology Vitamin D deficiency Histiocytosis Prolonged prothrombin time Cholangitis Ulcerative colitis Acute hepatic failure Hepatocellular carcinoma Amyloidosis Fetal ascites Generalized cerebral atrophy/hypoplasia Full cheeks Pulmonary granulomatosis Delayed speech and language development Cognitive impairment Cryptorchidism Pharyngitis Pyelonephritis Recurrent pharyngitis Severe failure to thrive Leukocytosis Psoriasiform dermatitis Progressive muscle weakness Ptosis Abnormal trabecular meshwork morphology Vitreous snowballs Intellectual disability, severe Enlarged lacrimal glands Abnormality of the nasal mucosa Increased T cell count Abnormal cardiac ventricular function Parotitis Abnormal liver parenchyma morphology Non-caseating epithelioid cell granulomatosis Abnormality of T cell physiology Enlargement of parotid gland Posterior vitreous detachment Abnormality of skin morphology Abnormal reproductive system morphology Intrauterine growth retardation Abnormality of the dentition Vitreous floaters Attention deficit hyperactivity disorder Sleep disturbance Tapered finger Short foot Small hand Downturned corners of mouth Short palm Infertility Genu valgum Carious teeth Hypermetropia Leukemia Stroke Apnea Intellectual disability, mild Abnormality of the nervous system Thin upper lip vermilion Narrow mouth Autism Micropenis Hyperactivity Hypogonadism Prominent forehead Hyporeflexia Clinodactyly Obesity Syndactyly Kyphosis Vitritis Abnormal conjunctiva morphology Blindness Osteolysis Elevated erythrocyte sedimentation rate Increased antibody level in blood Blurred vision Pulmonary fibrosis Emphysema Diabetes insipidus Epiphora Hypercalcemia Hypercalciuria Eosinophilia Ventricular tachycardia Leukopenia Nephrocalcinosis Hyperthyroidism Hyperpigmentation of the skin Nephrolithiasis Subcutaneous nodule Palpitations Syncope Sudden cardiac death Chest pain Papule Cough Erythema Facial palsy Glaucoma Alopecia Abnormality of the musculature Hyperuricemia Iridocyclitis Abnormality of the pleura Abnormal salivary gland morphology Anterior uveitis Dacryocystitis Chorioretinitis Abnormality of the adrenal glands Abnormality of the lymph nodes Skin plaque Erythema nodosum Abnormality of the cerebrospinal fluid Cystoid macular edema Chylothorax Vitreous hemorrhage Pneumothorax Keratoconjunctivitis sicca Anterior synechiae of the anterior chamber Night sweats Skin nodule Bone cyst Macular edema Upper airway obstruction Abnormality of the gastrointestinal tract Tubulointerstitial nephritis Increased CSF protein Heart block Joint swelling Optic neuropathy Hemoptysis Abnormality of blood glucose concentration



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