Anemia, and Vertigo

Diseases related with Anemia and Vertigo

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


Top matches:

Medium match ORTHOSTATIC HYPOTENSION 2; ORTHYP2


Orthostatic hypotension-2 is an autosomal recessive disorder characterized by severe orthostatic hypotension, recurrent hypoglycemia, and low norepinephrine levels. The disorder has onset in infancy or early childhood. Some patients may also have renal dysfunction and reduced life expectancy. The disorder results from a defect in the biosynthesis of norepinephrine from dopamine due to a cofactor deficiency.For a discussion of genetic heterogeneity of ORTHYP, see ORTHYP1 (OMIM ).

Related symptoms:

  • Anemia
  • Hypoglycemia
  • Vertigo
  • Tachycardia
  • Hypotension


SOURCES: OMIM MENDELIAN

More info about ORTHOSTATIC HYPOTENSION 2; ORTHYP2

Low 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

Low match JUVENILE POLYPOSIS SYNDROME; JPS


Juvenile polyposis syndrome is an autosomal dominant condition that predisposes gene carriers to various types of tumors. The diagnosis is based on the occurrence of hamartomatous gastrointestinal polyps that turn into malignant lesions in approximately 20% of cases (Handra-Luca et al., 2005).It had been suggested that juvenile polyposis can be caused by mutations in the PTEN gene (OMIM ), the same gene that is mutant in Cowden syndrome-1 (OMIM ). In a comprehensive review of PTEN, Waite and Eng (2002) concluded that juvenile intestinal polyposis is not a so-called PTEN hamartoma-tumor syndrome (PHTS). They suggested that the discovery of the germline PTEN mutation in an individual considered to have JPS should raise a suspicion that the clinical diagnosis is incorrect and that such an individual should be managed medically in the same manner as all patients with PHTS.

JUVENILE POLYPOSIS SYNDROME; JPS Is also known as polyposis, juvenile intestinal|pji|jip|juvenile intestinal polyposis|polyposis, familial, of entire gastrointestinal tract

Related symptoms:

  • Seizures
  • Neoplasm
  • Failure to thrive
  • Pain
  • Cryptorchidism


SOURCES: OMIM MENDELIAN

More info about JUVENILE POLYPOSIS SYNDROME; JPS

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Other less relevant matches:

Low match XFE PROGEROID SYNDROME; XFEPS


XFE PROGEROID SYNDROME; XFEPS Is also known as xpf-ercc1 progeroid syndrome

Related symptoms:

  • Hearing impairment
  • Microcephaly
  • Scoliosis
  • Ataxia
  • Neoplasm


SOURCES: MESH OMIM MENDELIAN

More info about XFE PROGEROID SYNDROME; XFEPS

Low match DEAFNESS-LYMPHEDEMA-LEUKEMIA SYNDROME


Deafness - lymphedema - leukemia is a very rare, serious syndromic genetic disorder characterized by primary lymphedema, immunodeficiency, and hematological disorders.

DEAFNESS-LYMPHEDEMA-LEUKEMIA SYNDROME Is also known as emberger syndrome

Related symptoms:

  • Hearing impairment
  • Neoplasm
  • Sensorineural hearing impairment
  • Anemia
  • Epicanthus


SOURCES: OMIM ORPHANET MENDELIAN

More info about DEAFNESS-LYMPHEDEMA-LEUKEMIA SYNDROME

Low match WALDENSTRÖM MACROGLOBULINEMIA


Waldenström macroglobulinemia (WM) is an indolent B-cell lymphoproliferative disorder characterized by the accumulation of monoclonal cells in the bone marrow and peripheral lymphoid tissues, and associated with the production of serum immunoglobulin M (IgM) monoclonal protein.

Related symptoms:

  • Hearing impairment
  • Ataxia
  • Neoplasm
  • Anemia
  • Peripheral neuropathy


SOURCES: OMIM ORPHANET MENDELIAN

More info about WALDENSTRÖM MACROGLOBULINEMIA

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 KEARNS-SAYRE SYNDROME


Kearns-Sayre syndrome (KSS) is a mitochondrial disease characterized by progressive external ophthalmoplegia (PEO), pigmentary retinitis and an onset before the age of 20 years. Common additional features include deafness, cerebellar ataxia and heart block.

KEARNS-SAYRE SYNDROME Is also known as ophthalmoplegia, pigmentary degeneration of retina, and cardiomyopathy|cpeo with myopathy|oculocraniosomatic syndrome|ophthalmoplegia, progressive external, with ragged-red fibers|cpeo with ragged-red fibers|chronic progressive external ophthalmoplegia wi

Related symptoms:

  • Seizures
  • Short stature
  • Generalized hypotonia
  • Hearing impairment
  • Microcephaly


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about KEARNS-SAYRE SYNDROME

Low match CAMURATI-ENGELMANN DISEASE


Camurati-Englemann disease (CED) is a rare, clinically variable bone dysplasia syndrome characterized by hyperostosis of the long bones, skull, spine and pelvis, associated with severe pain in the extremities, a wide-based waddling gait, joint contractures, muscle weakness and easy fatigability. Camurati-Englemann disease (CED) is a rare, clinically variable bone dysplasia syndrome characterized by hyperostosis of the long bones, skull, spine and pelvis, associated with severe pain in the extremities, a wide-based waddling gait, joint contractures, muscle weakness and easy fatigability.

CAMURATI-ENGELMANN DISEASE Is also known as diaphyseal dysplasia 1, progressive|engelmann disease|progressive diaphyseal dysplasia|dpd1|ced|pdd

Related symptoms:

  • Hearing impairment
  • Scoliosis
  • Ataxia
  • Muscle weakness
  • Abnormal facial shape


SOURCES: OMIM ORPHANET MENDELIAN

More info about CAMURATI-ENGELMANN DISEASE

Low match ERYTHROCYTOSIS, FAMILIAL, 5; ECYT5


Erythrocytosis-5 is an autosomal dominant clinical condition characterized by increased red cell mass and typically elevated hemoglobin concentration and hematocrit. Some patients have increased serum EPO levels (summary by Zmajkovic et al., 2018).For a general phenotypic description and a discussion of genetic heterogeneity of familial erythrocytosis, see ECYT1 (OMIM ).

Related symptoms:

  • Headache
  • Vertigo
  • Polycythemia
  • Increased hemoglobin
  • Increased hematocrit


SOURCES: OMIM MENDELIAN

More info about ERYTHROCYTOSIS, FAMILIAL, 5; ECYT5

Top 5 symptoms//phenotypes associated to Anemia and Vertigo

Symptoms // Phenotype % cases
Fatigue Common - Between 50% and 80% cases
Headache Uncommon - Between 30% and 50% cases
Neoplasm Uncommon - Between 30% and 50% cases
Splenomegaly Uncommon - Between 30% and 50% cases
Hearing impairment Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Anemia and Vertigo. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Ataxia Hepatomegaly Pain Elevated erythrocyte sedimentation rate Fever Vasculitis Weight loss Pallor Congestive heart failure Migraine Optic atrophy Muscle weakness Lymphadenopathy Diarrhea

Rare Symptoms - Less than 30% cases


Visual loss Recurrent infections Edema Cachexia Skeletal muscle atrophy Sensorineural hearing impairment Carious teeth Severe short stature Renal insufficiency Scoliosis Microcephaly Leukemia Bruising susceptibility Neurological speech impairment Memory impairment Muscular dystrophy Paralysis Sensory neuropathy Periorbital edema Raynaud phenomenon Cranial nerve paralysis Anorexia Proptosis Hypogonadism Peripheral neuropathy Erysipelas Hypercoagulability Cellulitis Polycythemia Leukopenia Bone marrow hypocellularity Leukocytosis Respiratory insufficiency Diplopia Seizures Hepatosplenomegaly Dyspnea Abdominal pain Hernia Respiratory distress Elevated hepatic transaminase Stroke Cirrhosis Chest pain Hypertension Gastrointestinal hemorrhage Myelodysplasia Epistaxis Sideroblastic anemia Incoordination Leukoencephalopathy Renal tubular acidosis Basal ganglia calcification Ventricular hypertrophy Left ventricular hypertrophy Bundle branch block Abnormality of retinal pigmentation Adrenal insufficiency EMG abnormality Cranial nerve compression Hemiplegia/hemiparesis External ophthalmoplegia Ophthalmoparesis Optic nerve compression Reduced tendon reflexes Diaphyseal sclerosis Diaphyseal dysplasia Ragged-red muscle fibers Abnormality of mitochondrial metabolism Ventricular arrhythmia Cerebral calcification Cortical sclerosis Atrioventricular block Craniofacial osteosclerosis Bilateral ptosis Nasal speech Cardiomegaly Muscle cramps Pigmentary retinopathy Dysphagia Hyporeflexia Arrhythmia Encephalopathy Depressivity Myopathy Blindness Cardiomyopathy Increased hemoglobin Elevated serum creatine phosphokinase Cognitive impairment Ptosis Muscular hypotonia Nystagmus Generalized hypotonia Short stature Fasciitis Delayed skeletal maturation Cerebellar hypoplasia Growth hormone deficiency Nyctalopia Syncope Primary adrenal insufficiency Lactic acidosis Limb muscle weakness Ophthalmoplegia Dilated cardiomyopathy Cortical thickening of long bone diaphyses Retinopathy Rod-cone dystrophy Abnormal subcutaneous fat tissue distribution Acidosis Hypothyroidism Reduced visual acuity Diabetes mellitus Elevated aldolase level Myoclonus Dementia Abnormality of the radius Increased CSF protein Exocrine pancreatic insufficiency Slender build Genu valgum Facial paralysis Delayed puberty Hyperlordosis Feeding difficulties in infancy Facial palsy Hypertrophic cardiomyopathy Limitation of joint mobility Abnormality of tibia morphology Abnormality of the nervous system Proximal muscle weakness Abnormality of femur morphology Difficulty walking Pes planus Skeletal dysplasia Delayed eruption of teeth Waddling gait Glaucoma Reduced subcutaneous adipose tissue Abnormality of the skull Poor appetite Aplasia/Hypoplasia of the radius Abnormality of the vertebral column Metaphyseal dysplasia Abnormality of the ulna Hyperostosis Lumbar hyperlordosis Abnormality of pelvic girdle bone morphology Easy fatigability Tinnitus Increased intracranial pressure Coxa valga Increased bone mineral density Bone pain Mandibular prognathia Hyperactivity Progressive external ophthalmoplegia Hypomagnesemia Abnormal diaphysis morphology Anterior hypopituitarism Stroke-like episode Gait imbalance Lower limb pain Severe lactic acidosis Hyperaldosteronism Urinary retention Heart block Sclerosis of skull base Mitochondrial myopathy Gangrene Cranial hyperostosis Hypoparathyroidism Limb pain Abnormality of the mitochondrion Abnormality of the humerus Extramedullary hematopoiesis Second degree atrioventricular block Kyphosis Frontal bossing Gait disturbance Flexion contracture Abnormal facial shape Low CSF 5-methyltetrahydrofolate Progressive intervertebral space narrowing Orchitis Titubation Third degree atrioventricular block Adrenocorticotropin deficient adrenal insufficiency Folate deficiency Otosclerosis Renal Fanconi syndrome First degree atrioventricular block Muscle fiber atrophy Hepatic amyloidosis Arthralgia Abnormality of the sacroiliac joint Ventriculomegaly Ascites Dry skin Proteinuria Deeply set eye Pneumonia Intellectual disability, mild Visual impairment Hypoplasia of dental enamel Cataract Hepatic vascular malformations Adenocarcinoma of the colon Duodenal adenocarcinoma Multiple gastric polyps Intussusception Melena Cutaneous photosensitivity Narrow face Hamartomatous polyposis Cerebellar atrophy Scarring Respiratory failure Recurrent respiratory infections Thrombocytopenia Immunodeficiency Syndactyly Epicanthus Neoplasm of the skin Lack of subcutaneous fatty tissue Bird-like facies Absence of subcutaneous fat Poor coordination Prematurely aged appearance High pitched voice Prominent supraorbital ridges Hematemesis Stomach cancer Hemolytic anemia Macrocytic anemia Hypolipidemia Abnormality of iron homeostasis Hypocholesterolemia Hypochromic microcytic anemia Anemia of inadequate production Megaloblastic anemia Microcytic anemia Failure to thrive Glucose intolerance Hyperpigmentation of the skin Falls Recurrent hypoglycemia Orthostatic hypotension Hypotension Tachycardia Thiamine-responsive megaloblastic anemia Cryptorchidism Rectal prolapse Portal hypertension Intestinal polyposis Clubbing of fingers Hematochezia Hemoptysis Hamartoma Colon cancer Clubbing Hypoalbuminemia Macrocephaly Hypokalemia Telangiectasia Cyanosis Cough Carcinoma Jaundice Umbilical hernia Nausea and vomiting Hematuria Conjunctival hyperemia Papule Muscle stiffness Meningitis Peripheral demyelination Hepatic failure Nausea Paresthesia Skin rash Intestinal obstruction Erythema Arthritis Myalgia Hypoglycemia Constipation Inguinal hernia Behavioral abnormality Conjunctivitis Hypermelanotic macule Polyclonal elevation of IgM Recurrent pharyngitis Optic neuritis Neuritis Pleuritis Chills Lymphocytosis Elevated C-reactive protein level Peritonitis Macule Abnormal myocardium morphology Myositis Reticulocytosis Uveitis Episodic fever Pericarditis Amyloidosis Vomiting Cryoglobulinemia Tapered finger Acute myeloid leukemia Macronodular cirrhosis Granulocytopenia Myeloproliferative disorder Abnormality of the optic nerve Verrucae Acute leukemia Myeloid leukemia Autoimmunity Prolonged bleeding time Chronic otitis media Intracranial hemorrhage Lymphedema Pancytopenia Hypotelorism Webbed neck Abnormal neutrophil count Malabsorption Impaired lymphocyte transformation with phytohemagglutinin Lymphoproliferative disorder Monoclonal immunoglobulin M proteinemia Multifocal epileptiform discharges Retinal hemorrhage Abnormality of neutrophils Normocytic anemia Reduced consciousness/confusion Abnormality of the retinal vasculature Edema of the lower limbs Polyneuropathy Pulmonary infiltrates Gingival bleeding Cutis marmorata Pleural effusion Urticaria Purpura Lymphoma Increased hematocrit



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