Anemia, and Migraine

Diseases related with Anemia and Migraine

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


Top matches:

Low match PAROXYSMAL EXERTION-INDUCED DYSKINESIA


Paroxysmal exertion-induced dyskinesia (PED) is a form of paroxysmal dyskinesia (see this term), characterized by painless attacks of dystonia of the extremities triggered by prolonged physical activities.

PAROXYSMAL EXERTION-INDUCED DYSKINESIA Is also known as ped with or without epilepsy and/or hemolytic anemia|paroxysmal exertion-induced dystonia with or without epilepsy and/or hemolytic anemia|dyt18|dystonia 18|ped|paroxysmal exercise-induced dyskinesia with or without epilepsy and/or hemolytic anemia

Related symptoms:

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


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about PAROXYSMAL EXERTION-INDUCED DYSKINESIA

Low match STORMORKEN-SJAASTAD-LANGSLET SYNDROME


Stormorken-Sjaastad-Langslet syndrome is characterized by thrombocytopathy, asplenia, miosis, muscle fatigue, migraine, dyslexia, and ichthyosis. It has been described in six members of one family. It is transmitted as an autosomal dominant trait.

STORMORKEN-SJAASTAD-LANGSLET SYNDROME Is also known as thrombocytopathy-asplenia-miosis syndrome|york platelet syndrome|thrombocytopathy, asplenia, and miosis|yps|stormorken syndrome

Related symptoms:

  • Short stature
  • Muscle weakness
  • Anemia
  • Fatigue
  • Myopathy


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about STORMORKEN-SJAASTAD-LANGSLET SYNDROME

Low match PHOSPHOGLYCERATE KINASE 1 DEFICIENCY


Phosphoglycerate kinase-1 deficiency is an X-linked recessive condition with a highly variable clinical phenotype that includes hemolytic anemia, myopathy, and neurologic involvement. Patients can express 1, 2, or all 3 of these manifestations (Shirakawa et al., 2006).

PHOSPHOGLYCERATE KINASE 1 DEFICIENCY Is also known as pgk1 deficiency

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Ataxia


SOURCES: MESH OMIM MENDELIAN

More info about PHOSPHOGLYCERATE KINASE 1 DEFICIENCY

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Other less relevant matches:

Low match HEREDITARY HEMORRHAGIC TELANGIECTASIA


Rendu-Osler-Weber disease, also called hereditary hemorrhagic telangiectasia (HHT), is a disorder of angiogenesis leading to arteriovenous dilatations: cutaneo-mucosal hemorrhagic telangiectasias and visceral shunting.

HEREDITARY HEMORRHAGIC TELANGIECTASIA Is also known as hht|rendu-osler disease|rendu-osler-weber disease

Related symptoms:

  • Seizures
  • Congestive heart failure
  • Cirrhosis
  • Hepatic failure
  • Hematuria


SOURCES: ORPHANET MENDELIAN

More info about HEREDITARY HEMORRHAGIC TELANGIECTASIA

Low match TAKAYASU ARTERITIS


Takayasu arteritis (TAK) is a rare inflammatory large-vessel vasculitis primarily affecting the aorta and its major branches, but also other large vessels, causing stenosis, occlusion, or aneurysm.

TAKAYASU ARTERITIS Is also known as young female arteritis|aortic arch syndrome|pulseless disease

Related symptoms:

  • Seizures
  • Muscle weakness
  • Anemia
  • Hypertension
  • Fever


SOURCES: ORPHANET OMIM MENDELIAN

More info about TAKAYASU ARTERITIS

Low match HERMANSKY-PUDLAK SYNDROME 6; HPS6


Related symptoms:

  • Global developmental delay
  • Hearing impairment
  • Nystagmus
  • Strabismus
  • Anemia


SOURCES: OMIM MENDELIAN

More info about HERMANSKY-PUDLAK SYNDROME 6; HPS6

Low match CINCA SYNDROME


Chronic Infantile Neurological, Cutaneous, and Articular (CINCA) syndrome is characterised by skin rash, joint involvement, chronic meningitis with granulocytes and, in some cases, sensorineural hearing loss and ocular signs.

CINCA SYNDROME Is also known as multisystem inflammatory disease, neonatal-onset|nomid syndrome|iomid syndrome|infantile-onset multisystem inflammatory disease|prieur-griscelli syndrome|neonatal-onset multisystem inflammatory disease|chronic neurologic cutaneous and articular syndrome|c

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Hearing impairment
  • Growth delay
  • Sensorineural hearing impairment


SOURCES: OMIM ORPHANET MENDELIAN

More info about CINCA SYNDROME

Low match TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1; HHT1


Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant vascular dysplasia leading to telangiectases and arteriovenous malformations of skin, mucosa, and viscera. Epistaxis and gastrointestinal bleeding are frequent complications of mucosal involvement. Visceral involvement includes that of the lung, liver, and brain. The most frequent form of hereditary hemorrhagic telangiectasia maps to the long arm of chromosome 9. Genetic Heterogeneity of Hereditary Hemorrhagic TelangiectasiaSee also HHT2 (OMIM ), caused by mutation in the ALK1 gene (ACVRL1 ) on chromosome 12q13; HHT3 (OMIM ), mapped to chromosome 5q31; HHT4 (OMIM ), mapped to chromosome 7p14; and HHT5 (OMIM ), caused by mutation in the GDF2 gene (OMIM ) on chromosome 10q11.See also juvenile polyposis/HHT syndrome (OMIM ), caused by mutation in the SMAD4 gene (OMIM ).

TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1; HHT1 Is also known as telangiectasia, hereditary hemorrhagic, of rendu, osler, and weber|orw disease|hht|osler-rendu-weber disease

Related symptoms:

  • Seizures
  • Anemia
  • Hypertension
  • Congestive heart failure
  • Headache


SOURCES: OMIM MENDELIAN

More info about TELANGIECTASIA, HEREDITARY HEMORRHAGIC, TYPE 1; HHT1

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

Top 5 symptoms//phenotypes associated to Anemia and Migraine

Symptoms // Phenotype % cases
Seizures Common - Between 50% and 80% cases
Epistaxis Uncommon - Between 30% and 50% cases
Fatigue Uncommon - Between 30% and 50% cases
Cirrhosis Uncommon - Between 30% and 50% cases
Subarachnoid hemorrhage Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Global developmental delay Myalgia Hematuria Conjunctival telangiectasia Gastrointestinal hemorrhage Pulmonary arterial hypertension Hemoptysis Transient ischemic attack Visual loss Splenomegaly Intellectual disability Fever Hypertension Cerebral hemorrhage Purpura Hearing impairment Headache Dilatation Muscle weakness Bruising susceptibility Neurological speech impairment Hemolytic anemia

Rare Symptoms - Less than 30% cases


Esophageal varix Dyspnea Encephalopathy Portal hypertension Congestive heart failure Hepatosplenomegaly Telangiectasia Brachydactyly Increased muscle fatiguability Abnormal thrombocyte morphology Hypotelorism Stroke Cyanosis Melena Ischemic stroke Gastrointestinal telangiectasia Leukocytosis Lymphadenopathy Nausea and vomiting Edema Hepatomegaly Sensorineural hearing impairment Prolonged bleeding time Inflammatory abnormality of the eye Vasculitis Arthritis Arthralgia Weight loss Fingerpad telangiectases Gastrointestinal arteriovenous malformation Nail bed telangiectasia Clubbing Palate telangiectasia Tongue telangiectasia Nasal mucosa telangiectasia Hepatic arteriovenous malformation Pulmonary arteriovenous malformation Spinal arteriovenous malformation Brain abscess Right-to-left shunt Gastrointestinal angiodysplasia Lip telangiectasia Cerebral arteriovenous malformation Spontaneous, recurrent epistaxis Hematemesis Polycythemia Skin rash Hematochezia Ataxia EEG abnormality Reticulocytosis Short stature Mental deterioration Thrombocytopenia Hemiplegia Myopathy Nystagmus Papule Skeletal dysplasia Proptosis Blindness Proximal muscle weakness Macrocephaly Spasticity Visual impairment Abnormal facial shape Cognitive impairment Frontal bossing Microcephaly Impaired ADP-induced platelet aggregation Premature birth Overgrowth Meningitis Joint dislocation Increased intracranial pressure Reduced bone mineral density Urticaria Generalized hypotonia Elevated erythrocyte sedimentation rate Progressive sensorineural hearing impairment Abnormal joint morphology Arthropathy Amyloidosis Growth delay Macular hypoplasia Abnormal platelet granules Recurrent urinary tract infections Amaurosis fugax Gastrointestinal infarctions Arteritis Hypertensive crisis Increased inflammatory response Dysarthria Strabismus Hernia Reduced visual acuity Photophobia Anal atresia Abnormal lung morphology Exotropia Absent foveal reflex Recurrent upper respiratory tract infections Albinism Hyperreflexia Interstitial pulmonary abnormality Colitis Iron deficiency anemia Congenital nystagmus Hypoplasia of the fovea Ocular albinism Generalized hypopigmentation Rotary nystagmus Partial albinism Endometriosis Uveitis Elevated C-reactive protein level Juvenile rheumatoid arthritis Bone marrow hypocellularity Syndactyly Immunodeficiency Recurrent infections Recurrent respiratory infections Respiratory failure Pallor Scarring Leukemia Vertigo Tapered finger Webbed neck Pancytopenia Lymphedema Leukopenia Respiratory insufficiency Intracranial hemorrhage Myelodysplasia Chronic otitis media Cellulitis Myeloid leukemia Acute myeloid leukemia Acute leukemia Hypercoagulability Verrucae Abnormality of the optic nerve Myeloproliferative disorder Granulocytopenia Erysipelas Macronodular cirrhosis Cerebellar atrophy Epicanthus Delayed closure of the anterior fontanelle Abnormality of the vasculature Ascending tubular aorta aneurysm Abnormality of neutrophils Pseudopapilledema Retrobulbar optic neuritis Abnormal granulocyte morphology Abnormality of the liver Nausea Ascites Atherosclerosis Elevated alkaline phosphatase Pericardial effusion Scleroderma Thrombocytosis Hypoxemia Neoplasm Migraine with aura Venous malformation Arteriovenous fistula Focal sensory seizure Polycystic liver disease Pulmonary hemorrhage Hemangiomatosis Coronary artery aneurysm Arteriovenous fistulas of celiac and mesenteric vessels High-output congestive heart failure Visual auras Venous varicosities of celiac and mesenteric vessels Dilatation of mesenteric artery Dilatation of celiac artery Abnormal endocardium morphology Reduced consciousness/confusion Arterial stenosis Myoglobinuria Paralysis Muscular dystrophy Retinal dystrophy Muscle cramps Tetraparesis Exercise intolerance Hyperbilirubinemia Spastic tetraparesis Emotional lability Aphasia Rhabdomyolysis Acute kidney injury Progressive encephalopathy Decreased mean corpuscular volume Jaundice Recurrent myoglobinuria Exercise-induced muscle cramps Exercise-induced myoglobinuria Limb dysmetria Migraine without aura Hepatic failure Abnormality of the head Torsion dystonia Episodic ataxia Nephrolithiasis Amblyopia Venous thrombosis Cholelithiasis Paroxysmal dyskinesia Rod-cone dystrophy Hand tremor Stroke-like episode High forehead Limb muscle weakness Ichthyosis Severe short stature Abnormal bleeding Prominent nose Elevated serum creatine phosphokinase Hypocalcemia Abnormality of coagulation Abnormality of the musculature Mitochondrial myopathy Asplenia Dyslexia Generalized tonic-clonic seizures without focal onset Paroxysmal dystonia Miosis Hypoglycorrhachia Increased mean platelet volume Abnormal platelet morphology Upgaze palsy Congenital miosis Pain High palate Delayed speech and language development Upper limb dysmetria Focal aware seizure Renal insufficiency Jerky head movements Action tremor Microcytic anemia Abnormal pattern of respiration Retinopathy Paresthesia Dysmetria Abnormality of movement Generalized tonic-clonic seizures Irritability Intellectual disability, moderate Aggressive behavior Gait ataxia Hyperhidrosis Myoclonus Cerebral atrophy Intellectual disability, mild Hypertrophic cardiomyopathy Chest pain Dyskinesia Myocardial infarction Subcutaneous nodule Anorexia Skin ulcer Dystonia Aortic regurgitation Psoriasiform dermatitis Abnormal heart valve morphology Gangrene Cerebral ischemia Deeply set eye Abnormal aortic valve morphology Tremor Falls Chorea Telangiectasia of the skin Mucosal telangiectasiae Pulmonary embolism Hyperactive deep tendon reflexes Arteriovenous malformation Abnormality of the cerebral vasculature Atonic seizures Intestinal polyposis Visceral angiomatosis Cavernous hemangioma Impulsivity Cholecystitis Spontaneous hematomas Abnormality of cardiovascular system physiology Peripheral arteriovenous fistula Retinal telangiectasia Choriocapillaris atrophy Focal impaired awareness seizure Slurred speech Absence seizures Horizontal nystagmus Progressive microcephaly Limb ataxia Lower limb spasticity Frequent falls Involuntary movements Choreoathetosis Generalized-onset seizure Specific learning disability Focal-onset seizure Abnormal neutrophil count



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Ventricular septal defect and Microphthalmia, related diseases and genetic alterations Fever and Anal atresia, related diseases and genetic alterations Hyperreflexia and Hyporeflexia, related diseases and genetic alterations Edema and Muscle cramps, related diseases and genetic alterations Failure to thrive and Bruising susceptibility, related diseases and genetic alterations

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