Anemia, and Headache

Diseases related with Anemia and Headache

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


Top matches:

Low match OSTEOPETROSIS, AUTOSOMAL DOMINANT 3; OPTA3


Autosomal dominant osteopetrosis-3 is characterized by phenotypic variability. Some patients have typical features of osteopetrosis, including fractures after minor trauma, early tooth loss, anemia, hepatosplenomegaly, and a generalized increase in bone mineral density, whereas other patients exhibit localized osteosclerosis and generalized osteopenia. OPTA3 represents a relatively malignant form of osteopetrosis in some patients who develop significant pancytopenia and hepatosplenomegaly (Bo et al., 2016).For a discussion of genetic heterogeneity of autosomal dominant osteopetrosis, see OPTA1 (OMIM ).

Related symptoms:

  • Anemia
  • Fatigue
  • Headache
  • Osteoporosis
  • Osteopenia


SOURCES: OMIM MENDELIAN

More info about OSTEOPETROSIS, AUTOSOMAL DOMINANT 3; OPTA3

Low match MALARIA


Malaria is a preventable life-threatening parasitic disease caused by Plasmodium (P. ) parasites that are transmitted by Anophles mosquito bites to humans and is typically clinically characterized by attacks of fever, headache, chills and vomiting.

Related symptoms:

  • Cognitive impairment
  • Anemia
  • Fever
  • Respiratory distress
  • Headache


SOURCES: OMIM ORPHANET MENDELIAN

More info about MALARIA

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Other less relevant matches:

Low match ACQUIRED IDIOPATHIC SIDEROBLASTIC ANEMIA


Acquired idiopathic sideroblastic anaemia is one of a group of disorders known as the myelodysplastic syndromes (MDS) characterised by ineffective haemopoiesis affecting one or more blood cell lineages (myeloid, erythroid or megakaryocytic) leading to peripheral blood cytopenias and an increased risk of developing leukaemia. Acquired idiopathic sideroblastic anaemia is now more commonly referred to as refractory anaemia with ringed sideroblasts or the acronym RARS.

ACQUIRED IDIOPATHIC SIDEROBLASTIC ANEMIA Is also known as rars|primary acquired sideroblastic anemia|refractory anemia with ringed sideroblasts|aisa

Related symptoms:

  • Pain
  • Anemia
  • Fatigue
  • Respiratory distress
  • Congestive heart failure


SOURCES: OMIM ORPHANET MENDELIAN

More info about ACQUIRED IDIOPATHIC SIDEROBLASTIC ANEMIA

Low match HEREDITARY SPHEROCYTOSIS


Hereditary spherocytosis is a congenital hemolytic anemia with a wide clinical spectrum (from symptom-free carriers to severe hemolysis) characterized by anemia, variable jaundice, splenomegaly and cholelithiasis.

HEREDITARY SPHEROCYTOSIS Is also known as sph|hs|minkowski-chauffard disease|hs1|spherocytosis, hereditary, 1

Related symptoms:

  • Short stature
  • Anemia
  • Fatigue
  • Abnormality of the skeletal system
  • Cardiomyopathy


SOURCES: ORPHANET OMIM MENDELIAN

More info about HEREDITARY SPHEROCYTOSIS

Low match CARNEY TRIAD


Carney's triad is a rare non-hereditary condition characterized by gastrointestinal stromal tumors (GIST, intramural mesenchymal tumors of the gastrointestinal tract with neuronal or neural crest cell origin), pulmonary chondromas and extraadrenal paragangliomas.

CARNEY TRIAD Is also known as gastric leiomyosarcoma, pulmonary chondroma, and extraadrenal paraganglioma

Related symptoms:

  • Anemia
  • Hypertension
  • Fatigue
  • Diarrhea
  • Headache


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about CARNEY TRIAD

Low match CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE III


Congenital dyserythropoietic anemia type III (CDA III) is a rare form of CDA (see this term) characterized by dyserythropoiesis, with big multinucleated erythroblasts in the bone marrow, and manifesting with mild to moderate anemia.

CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE III Is also known as anemia with multinucleated erythroblasts|erythroreticulosis, hereditary benign|congenital dyserythropoietic anemia type 3|cda type 3|dyserythropoietic anemia, congenital, type iii|cda iii|cda type iii

Related symptoms:

  • Short stature
  • Neoplasm
  • Anemia
  • Fatigue
  • Headache


SOURCES: ORPHANET OMIM MENDELIAN

More info about CONGENITAL DYSERYTHROPOIETIC ANEMIA TYPE III

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 HYPERTROPHIC CARDIOMYOPATHY AND RENAL TUBULAR DISEASE DUE TO MITOCHONDRIAL DNA MUTATION


Hypertrophic cardiomyopathy and renal tubular disease due to mitochondrial DNA mutation is a mitochondrial oxidative phosphorylation disorder characterized by hypertrophic and dilated cardiomyopathy, failure to thrive, myopathy with generalized hypotonia and increased creatine kinase, developmental delay and/or regression with cerebral atrophy on brain MRI, renal manifestations including chronic renal failure, renal tubular acidosis and lactic acidosis. Additional clinical features include seizures and respiratory failure.

HYPERTROPHIC CARDIOMYOPATHY AND RENAL TUBULAR DISEASE DUE TO MITOCHONDRIAL DNA MUTATION Is also known as hypertrophic cardiomyopathy and renal tubular disease due to mtdna mutation

Related symptoms:

  • Short stature
  • Hearing impairment
  • Sensorineural hearing impairment
  • Anemia
  • Hepatomegaly


SOURCES: ORPHANET MENDELIAN

More info about HYPERTROPHIC CARDIOMYOPATHY AND RENAL TUBULAR DISEASE DUE TO MITOCHONDRIAL DNA MUTATION

Low match PITUITARY APOPLEXY


The sudden loss of blood supply to the PITUITARY GLAND, leading to tissue NECROSIS and loss of function (PANHYPOPITUITARISM). The most common cause is hemorrhage or INFARCTION of a PITUITARY ADENOMA. It can also result from acute hemorrhage into SELLA TURCICA due to HEAD TRAUMA; INTRACRANIAL HYPERTENSION; or other acute effects of central nervous system hemorrhage. Clinical signs include severe HEADACHE; HYPOTENSION; bilateral visual disturbances; UNCONSCIOUSNESS; and COMA.

Related symptoms:

  • Ptosis
  • Hypertension
  • Fever
  • Fatigue
  • Headache


SOURCES: MESH ORPHANET MENDELIAN

More info about PITUITARY APOPLEXY

Top 5 symptoms//phenotypes associated to Anemia and Headache

Symptoms // Phenotype % cases
Fatigue Common - Between 50% and 80% cases
Hemolytic anemia Uncommon - Between 30% and 50% cases
Pallor Uncommon - Between 30% and 50% cases
Hyperbilirubinemia Uncommon - Between 30% and 50% cases
Nausea and vomiting Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Short stature

Rare Symptoms - Less than 30% cases


Irritability Arrhythmia Palpitations Respiratory distress Fever Cognitive impairment Tachycardia Hypertrophic cardiomyopathy Pain Jaundice Hypertension Diarrhea Abdominal pain Reticulocytosis Dyspnea Hepatosplenomegaly Episodic ataxia Torsion dystonia Abnormality of the head Migraine without aura Limb dysmetria Paroxysmal dyskinesia Abnormality of the kidney Hearing impairment Sensorineural hearing impairment Jerky head movements Proteinuria Diabetes mellitus Renal insufficiency Focal aware seizure Upper limb dysmetria Hypoglycorrhachia Hepatomegaly Generalized tonic-clonic seizures without focal onset Paroxysmal dystonia Focal impaired awareness seizure Action tremor Involuntary movements Abnormality of movement Dysmetria Paresthesia Falls Dyskinesia Chorea Migraine Focal-onset seizure Specific learning disability Generalized-onset seizure Choreoathetosis Frequent falls Hand tremor Lower limb spasticity Limb ataxia Progressive microcephaly Horizontal nystagmus Absence seizures Slurred speech Hemiplegia Hematuria Impulsivity Atonic seizures Hyperactive deep tendon reflexes Nephropathy Tubulointerstitial fibrosis Cardiomegaly Adrenocorticotropic hormone deficiency Blurred vision Hypopituitarism Growth hormone excess Increased circulating cortisol level Oligomenorrhea Prolactin excess Pituitary adenoma Excessive daytime somnolence Pituitary hypothyroidism Central diabetes insipidus Hyponatremia Normochromic anemia Galactorrhea Abnormality of the cerebrospinal fluid Mydriasis Prolactin deficiency Trigeminal neuralgia Bitemporal hemianopia Abnormal kinetic perimetry test Thunderclap headache Abnormal caudate nucleus morphology Impotence Cranial nerve paralysis Left ventricular hypertrophy Abnormal mitochondrial shape Ragged-red muscle fibers Pleural effusion Focal segmental glomerulosclerosis Glomerulopathy Tubular atrophy Increased CSF lactate Abnormal renal physiology Mental deterioration Peripheral edema Abnormal mitochondrial morphology Global glomerulosclerosis Hypergonadotropic hypogonadism Abnormal mitochondrial number Ptosis Reduced visual acuity Photophobia Hypoglycemia Confusion Coma Growth hormone deficiency Hypotension Diplopia Generalized tonic-clonic seizures Muscle weakness Intellectual disability, moderate Refractory sideroblastic anemia Congestive heart failure Chest pain Microcytic anemia Increased serum ferritin Decreased mean corpuscular volume Sideroblastic anemia Abnormal glucose tolerance Hypochromic anemia Crackles Abnormality of the skeletal system Elevated C-reactive protein level Cardiomyopathy Splenomegaly Erythema Delayed puberty Cholelithiasis Autoimmune hemolytic anemia Spherocytosis Elliptocytosis Erythroid hypoplasia Lymphadenopathy Morphological abnormality of the central nervous system Gait imbalance Gastrointestinal hemorrhage Rickets Arthralgia Urticaria Paroxysmal nocturnal hemoglobinuria Osteoporosis Osteopenia Pectus carinatum Recurrent fractures Pancytopenia Increased bone mineral density Hyperostosis Reduced consciousness/confusion Agenesis of permanent teeth Thickened calvaria Premature loss of teeth Osteopetrosis Generalized osteosclerosis Thrombocytopenia Myalgia Retinopathy Abnormality of blood and blood-forming tissues Acute kidney injury Ascites Anorexia Aggressive behavior Ataxia Increased total iron binding capacity Abnormal proerythroblast morphology Abnormal erythroid lineage cell morphology Hemosiderinuria Intellectual disability Seizures Global developmental delay Generalized hypotonia Microcephaly Nystagmus Post-partum hemorrhage Spasticity Hyperreflexia Dysarthria Tremor Dystonia Intellectual disability, mild Cerebral atrophy Myoclonus Gait ataxia EEG abnormality Oral cavity bleeding Abnormal cellular phenotype Pulmonary infiltrates Heterotopia Pheochromocytoma Paraganglioma Adrenocortical adenoma Mediastinal lymphadenopathy Leiomyosarcoma Gastrointestinal stroma tumor Adrenal overactivity Neoplasm Proptosis Elevated hepatic transaminase Macrocytic anemia Abnormal erythrocyte morphology Gingival bleeding Anisocytosis Increased mean corpuscular volume Multiple myeloma Anemia of inadequate production Poikilocytosis Melena Congenital hypoplastic anemia Erythroid hyperplasia Increased serum iron Abnormal static automated perimetry test



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