Anemia, and Anxiety

Diseases related with Anemia and Anxiety

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

Top matches:

Trimethylaminuria results from the abnormal presence of large amounts of volatile and malodorous trimethylamine within the body. This chemical, a tertiary aliphatic amine, is excreted in the urine, sweat (ichthyohidrosis), and breath, which take on the offensive odor of decaying fish (Mitchell, 1996).

TRIMETHYLAMINURIA; TMAU Is also known as fish-odor syndrome

Related symptoms:

  • Anemia
  • Hypertension
  • Splenomegaly
  • Depressivity
  • Hyperhidrosis


SOURCES: OMIM ORPHANET MENDELIAN

More info about TRIMETHYLAMINURIA; TMAU

Related symptoms:

  • Anemia
  • Fatigue
  • Thrombocytopenia
  • Depressivity
  • Anxiety


SOURCES: OMIM MENDELIAN

More info about THROMBOCYTOPENIA, CYCLIC

Hematologically, McLeod syndrome is characterized by the absence of red blood cell Kx antigen, weak expression of Kell red blood cell antigens, acanthocytosis, and compensated hemolysis. Most carriers of this McLeod blood group phenotype have acanthocytosis and elevated serum creatine kinase levels and are prone to develop a severe neurologic disorder resembling Huntington disease (OMIM ). Onset of neurologic symptoms ranges between 25 and 60 years (mean onset 30-40 years), and penetrance appears to be high. Additional symptoms include generalized seizures, neuromuscular symptoms leading to weakness and atrophy, and cardiomyopathy mainly manifesting with atrial fibrillation, malignant arrhythmias, and dilated cardiomyopathy (summary by Jung et al., 2007).The cooccurrence of McLeod syndrome and chronic granulomatous disease (CGD ) results from a contiguous gene deletion (Francke et al., 1985).

MCLEOD SYNDROME; MCLDS Is also known as mcleod phenotype|neuroacanthocytosis, mcleod type

Related symptoms:

  • Seizures
  • Muscle weakness
  • Cognitive impairment
  • Anemia
  • Peripheral neuropathy


SOURCES: MESH OMIM MENDELIAN

More info about MCLEOD SYNDROME; MCLDS

Other less relevant matches:

Acute intermittent porphyria is the most frequent and the most severe form of the acute hepatic porphyrias (see this term). It is characterized by the occurrence of neuro-visceral attacks without cutaneous manifestations.

ACUTE INTERMITTENT PORPHYRIA Is also known as ups deficiency|porphyria, swedish type|pbgd deficiency|porphobilinogen deaminase deficiency|uroporphyrinogen synthase deficiency

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Muscle weakness
  • Pain


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about ACUTE INTERMITTENT PORPHYRIA

Hereditary coproporphyria is a form of acute hepatic porphyria (see this term) characterized by the occurrence of neuro-visceral attacks and, more rarely, by the presence of cutaneous lesions.

HEREDITARY COPROPORPHYRIA Is also known as cpox deficiency|cpx deficiency|coproporphyrinogen oxidase deficiency|cpo deficiency

Related symptoms:

  • Seizures
  • Muscle weakness
  • Pain
  • Anemia
  • Hypertension


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about HEREDITARY COPROPORPHYRIA

McLeod neuroacanthocytosis syndrome (MLS) is a form of neuroacanthocytosis (see this term) and is characterized clinically by a Huntington's disease-like phenotype with an involuntary hyperkinetic movement disorder, psychiatric manifestations and cognitive alterations, and biochemically by absence of the Kx antigen and by weak expression of the Kell antigens.

MCLEOD NEUROACANTHOCYTOSIS SYNDROME Is also known as mls|x-linked mcleod syndrome

Related symptoms:

  • Seizures
  • Short stature
  • Muscle weakness
  • Cognitive impairment
  • Anemia


SOURCES: ORPHANET OMIM MENDELIAN

More info about MCLEOD NEUROACANTHOCYTOSIS SYNDROME

Juvenile Huntington disease (JHD) is a form of Huntington disease (HD; see this term), characterized by onset of signs and symptoms before 20 years of age.

JUVENILE HUNTINGTON DISEASE Is also known as huntington chorea|jhd|juvenile huntington chorea

Related symptoms:

  • Seizures
  • Ataxia
  • Cognitive impairment
  • Anemia
  • Delayed speech and language development


SOURCES: OMIM ORPHANET MENDELIAN

More info about JUVENILE HUNTINGTON DISEASE

Celiac disease, also known as celiac sprue and gluten-sensitive enteropathy (GSE), is a multifactorial disorder of the small intestine that is influenced by both environmental and genetic factors. It is characterized by malabsorption resulting from inflammatory injury to the mucosa of the small intestine after the ingestion of wheat gluten or related rye and barley proteins (summary by Farrell and Kelly, 2002). Long regarded as gastrointestinal disorder of childhood, the disease is now considered to be a chronic systemic autoimmune disease and is more often diagnosed in adults than in children (Monsuur et al., 2005).For a discussion of genetic heterogeneity of celiac disease, see MAPPING.

CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1 Is also known as celiac sprue, susceptibility to, 1|gluten-sensitive enteropathy, susceptibility to, 1

Related symptoms:

  • Seizures
  • Short stature
  • Ataxia
  • Failure to thrive
  • Anemia


SOURCES: OMIM MENDELIAN

More info about CELIAC DISEASE, SUSCEPTIBILITY TO, 1; CELIAC1

Wolfram syndrome-1 is a rare and severe autosomal recessive neurodegenerative disease characterized by diabetes mellitus, optic atrophy, diabetes insipidus, and deafness (DIDMOAD). Additional clinical features may include renal abnormalities, ataxia, dementia or mental retardation, and diverse psychiatric illnesses. The minimal diagnostic criteria for Wolfram syndrome are optic atrophy and diabetes mellitus of juvenile onset. Hearing impairment in Wolfram syndrome is typically progressive and mainly affects the higher frequencies, but a small fraction of affected individuals have congenital deafness (summary by Rendtorff et al., 2011).Autosomal dominant mutations in the WFS1 gene have been found to cause low-frequency nonsyndromic deafness (OMIM ) as well as a Wolfram syndrome-like phenotype (OMIM ) in which affected individuals have hearing impairment with diabetes mellitus and/or optic atrophy. Genetic Heterogeneity of Wolfram SyndromeWolfram syndrome-2 (WFS2 ) is caused by mutation in the CISD2 gene (OMIM ) on chromosome 4q24.

WOLFRAM SYNDROME 1; WFS1 Is also known as diabetes insipidus and mellitus with optic atrophy and deafness|wfs|didmoad

Related symptoms:

  • Intellectual disability
  • Seizures
  • Hearing impairment
  • Ataxia
  • Growth delay


SOURCES: OMIM MENDELIAN

More info about WOLFRAM SYNDROME 1; WFS1

Beta-thalassemia (BT) major is a severe early-onset form of BT (see this term) characterized by severe anemia requiring regular red blood cell transfusions.

BETA-THALASSEMIA MAJOR Is also known as cooley anemia|mediterranean anemia

Related symptoms:

  • Hearing impairment
  • Muscle weakness
  • Cataract
  • Anemia
  • Feeding difficulties


SOURCES: ORPHANET MENDELIAN

More info about BETA-THALASSEMIA MAJOR

Top 5 symptoms//phenotypes associated to Anemia and Anxiety

Symptoms // Phenotype % cases
Depressivity Very Common - Between 80% and 100% cases
Seizures Common - Between 50% and 80% cases
Behavioral abnormality Common - Between 50% and 80% cases
Muscle weakness Uncommon - Between 30% and 50% cases
Arrhythmia Uncommon - Between 30% and 50% cases

Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases

Arthralgia Weight loss Paresthesia Hypertension Hepatosplenomegaly Elevated hepatic transaminase Cardiomyopathy Dysarthria Diarrhea Peripheral neuropathy Cognitive impairment Hepatomegaly Splenomegaly Vomiting Psychosis Abnormal bleeding Myoclonus Chorea Generalized-onset seizure Areflexia Dementia Dystonia Dysphagia Ataxia Neutropenia Hallucinations Obsessive-compulsive behavior Fatigue Insomnia Rigidity Diabetes mellitus Tachycardia Irritability Hyperhidrosis Abdominal pain Constipation

Rare Symptoms - Less than 30% cases

Abdominal distention Cutaneous photosensitivity Type I diabetes mellitus Nausea Nausea and vomiting Paralysis Myalgia Hyponatremia Cataract Restlessness Acute episodes of neuropathic symptoms Abnormality of movement Hypothyroidism Neuronal loss in central nervous system Hemolytic anemia Confusion Involuntary movements Mental deterioration Jaundice Red urine Ileus Paranoia Dyspnea Hearing impairment Short stature Sleep apnea Gait disturbance Respiratory paralysis Abnormality of the cerebral white matter Delirium Personality changes Pain Tremor Rhabdomyolysis Myopathy Aggressive behavior Elevated serum creatine phosphokinase Infertility Neurodegeneration Osteoporosis Dilated cardiomyopathy Dyskinesia Atrial fibrillation Abnormal blistering of the skin Malabsorption Delayed puberty Falls Testicular atrophy Motor axonal neuropathy Cerebral atrophy Acanthocytosis Tics Intellectual disability Personality disorder Thrombocytopenia Chronic bronchitis Bronchitis Frequent temper tantrums Suicidal ideation Hypokinesia Neuronal loss in basal ganglia Abnormal involuntary eye movements Muscle fibrillation Recurrent aphthous stomatitis Cerebellar vermis atrophy Mania Prolonged prothrombin time Abnormality of the abdominal wall Upper limb undergrowth Folate deficiency Prolonged partial thromboplastin time Dilated fourth ventricle Head tremor Stomatitis Eczema Oral motor hypotonia Abnormality of the coagulation cascade Cerebral calcification Lymphoma Nevus Hypoplasia of dental enamel Chronic diarrhea Hypocalcemia Polyneuropathy Spontaneous abortion Abnormal intestine morphology Rickets Autoimmunity Malnutrition Failure to thrive Postnatal growth retardation Steatorrhea Celiac disease Macrocytic anemia IgA deficiency Thyroiditis Iron deficiency anemia Inflammatory abnormality of the skin Thrombocytosis Alopecia Chronic fatigue Vitamin D deficiency Abnormality of the urinary system Vitamin K deficiency Depressed nasal bridge Nyctalopia Pallor Skeletal dysplasia Upslanted palpebral fissure Abnormality of the dentition Fever Visual impairment Cirrhosis Feeding difficulties Limited mobility of proximal interphalangeal joint Impaired collagen-induced platelet aggregation Diffuse leukoencephalopathy Central sleep apnea Gastric ulcer Genu valgum Pulmonary arterial hypertension Sideroblastic anemia Abnormality of the skull Monochromacy Hypersplenism Abnormal hemoglobin Abnormality of the hypothalamus-pituitary axis Neoplasm of the liver Cardiorespiratory arrest Increased serum ferritin Skin ulcer Hypoparathyroidism Microcytic anemia Adrenal insufficiency Abnormality of the thorax Cholelithiasis Venous thrombosis Abnormal glucose tolerance Pollakisuria Vitamin B12 deficiency Hypogonadism Dehydration Vesicoureteral reflux Apnea Abnormality of the nervous system Hydronephrosis Respiratory failure Dilatation Hypergonadotropic hypogonadism Blindness Optic atrophy Ptosis Sensorineural hearing impairment Nystagmus Growth delay Pigmentary retinopathy Leukoencephalopathy Respiratory arrest Dyschromatopsia Central diabetes insipidus Histiocytosis Stroke-like episode Neurogenic bladder Central apnea Megaloblastic anemia Severe sensorineural hearing impairment Anosmia Atrophy/Degeneration affecting the brainstem Polyphagia Blurred vision Hydroureter Diabetes insipidus Rheumatoid arthritis Akinesia Ventricular extrasystoles Slurred speech Hepatocellular carcinoma Renal insufficiency Carcinoma Lethargy Stage 5 chronic kidney disease Nephropathy Coma Urinary incontinence Anorexia Paraparesis Hyperlipidemia Cranial nerve paralysis Apathy Agitation Dysuria Global developmental delay Urinary retention Diaphragmatic paralysis Abnormal urinary color Psychotic episodes Hypertensive crisis Paralytic ileus Elevated urinary delta-aminolevulinic acid Abnormality of metabolism/homeostasis Acidosis Pruritus Metabolic acidosis Hypotension Hypertrichosis Intellectual disability, mild Phonic tics Hypermelanotic macule Petechiae Abnormality of the cardiovascular system Recurrent pneumonia Alzheimer disease Body odor Fish odor Trimethylaminuria Skin rash Bruising susceptibility Gastrointestinal hemorrhage Epistaxis Purpura Intracranial hemorrhage Cerebral hemorrhage Thromboembolism Abetalipoproteinemia Autoimmune thrombocytopenia Gingival bleeding Arterial thrombosis Internal hemorrhage Cyclic neutropenia Skeletal muscle atrophy Pneumonia Muscular dystrophy Ichthyosis Cardiomegaly Aspiration EMG abnormality Abnormality of the musculature Aspiration pneumonia Thin skin Orthostatic hypotension Incoordination Gait ataxia Abnormal lactate dehydrogenase activity Caudate atrophy Abnormal corpus striatum morphology Recurrent singultus Blood group antigen abnormality Abnormal facial expression Hyporeflexia of upper limbs Abnormality of the astrocytes Delayed speech and language development Hyperreflexia Ventriculomegaly Cerebellar atrophy Hyperactivity Arthritis Impaired temperature sensation Cough Abnormality of eye movement Abnormal cerebellum morphology Progressive cerebellar ataxia Gliosis Brain atrophy Bradykinesia Type II diabetes mellitus Progressive neurologic deterioration Broad-based gait Clumsiness Schizophrenia Hyperkinesis Abnormal social behavior Generalized limb muscle atrophy Prolonged neonatal jaundice Left ventricular hypertrophy Fragile skin Visual hallucinations Auditory hallucinations Congenital hemolytic anemia Compensated hemolytic anemia Abdominal colic Hypertonia Congestive heart failure Babinski sign Lower limb muscle weakness Sensory neuropathy Parkinsonism Memory impairment Sensorimotor neuropathy Increased muscle fatiguability Cardiac arrest Ventricular arrhythmia Emotional lability Ventricular fibrillation Sensory axonal neuropathy Bowel incontinence Impaired vibration sensation in the lower limbs Impaired pain sensation Bipolar affective disorder Left bundle branch block Supraventricular tachycardia Orofacial dyskinesia Excessive salivation Hyporeflexia of lower limbs Malar prominence


If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Abnormality of the skeletal system and Brachycephaly, related diseases and genetic alterations Autoimmunity and Macroglossia, related diseases and genetic alterations High palate and Feeding difficulties in infancy, related diseases and genetic alterations Low-set ears and Confusion, related diseases and genetic alterations Ptosis and Hirsutism, related diseases and genetic alterations