Anemia, and Hyperhidrosis

Diseases related with Anemia and Hyperhidrosis

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


Top matches:

Low match TRIMETHYLAMINURIA; TMAU


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

Low match MALT LYMPHOMA


MALT (mucosa-associated lymphoid tissue) lymphoma is a rare form of malignant non-Hodgkin lymphoma (see this term) that affects B cells and grows at the expense of lymphoid tissue associated with mucous membranes, but also occurs, more rarely, in lymph nodes.

MALT LYMPHOMA Is also known as maltoma|mucosa-associated lymphatic tissue lymphoma|extranodal marginal zone b-cell lymphoma|mucosa-associated lymphoid tissue lymphoma

Related symptoms:

  • Anemia
  • Visual impairment
  • Fever
  • Fatigue
  • Constipation


SOURCES: ORPHANET MENDELIAN

More info about MALT LYMPHOMA

Low match BLUE RUBBER BLEB NEVUS


Blue rubber bleb nevus (BRBNS) is a rare vascular malformation disorder with cutaneous and visceral lesions frequently associated with serious, potentially fatal bleeding and anemia.

BLUE RUBBER BLEB NEVUS Is also known as brbn|bean syndrome

Related symptoms:

  • Growth delay
  • Neoplasm
  • Pain
  • Anemia
  • Thrombocytopenia


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about BLUE RUBBER BLEB NEVUS

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Other less relevant matches:

Low match AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK


Autoinflammation with arthritis and dyskeratosis is characterized by recurrent fever, widespread skin dyskeratosis, arthritis, elevated biologic markers of inflammation, and mild autoimmunity with a high transitional B-cell level (summary by Grandemange et al., 2016).

Related symptoms:

  • Growth delay
  • Failure to thrive
  • Anemia
  • Fever
  • Respiratory insufficiency


SOURCES: OMIM MENDELIAN

More info about AUTOINFLAMMATION WITH ARTHRITIS AND DYSKERATOSIS; AIADK

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 ACUTE INTERMITTENT PORPHYRIA


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

Low match PEUTZ-JEGHERS SYNDROME; PJS


Peutz-Jeghers syndrome is an autosomal dominant disorder characterized by melanocytic macules of the lips, buccal mucosa, and digits; multiple gastrointestinal hamartomatous polyps; and an increased risk of various neoplasms.

PEUTZ-JEGHERS SYNDROME; PJS Is also known as polyps-and-spots syndrome|polyposis, hamartomatous intestinal

Related symptoms:

  • Neoplasm
  • Hypertension
  • Edema
  • Diarrhea
  • Headache


SOURCES: OMIM MENDELIAN

More info about PEUTZ-JEGHERS SYNDROME; PJS

Low match NAKAJO-NISHIMURA SYNDROME


Nakajo-Nishimura syndrome (NNS) is a rare autoinflammatory disorder belonging to the proteasome disability syndrome (see this term) group, and characterized by pernio-like lesions appearing in infancy followed by recurrent fever, nodular skin eruption, partial lipodystrophy (mainly in upper extremities and face) and joint contractures.

NAKAJO-NISHIMURA SYNDROME Is also known as nns|secondary hypertrophic osteoperiostosis with pernio|amyotrophy-fat tissue anomaly syndrome

Related symptoms:

  • Muscle weakness
  • Hepatomegaly
  • Fever
  • Skeletal muscle atrophy
  • Respiratory insufficiency


SOURCES: ORPHANET MENDELIAN

More info about NAKAJO-NISHIMURA SYNDROME

Low match MCLEOD NEUROACANTHOCYTOSIS SYNDROME


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

Low match HYPERLIPOPROTEINEMIA, TYPE I


HYPERLIPOPROTEINEMIA, TYPE I Is also known as lpl deficiency|hyperchylomicronemia, familial|lipase d deficiency|lipd deficiency|lipoprotein lipase deficiency|hyperlipemia, essential familial|chylomicronemia, familial|hyperlipemia, idiopathic, burger-grutz type|hyperlipoproteinemia, type ia

Related symptoms:

  • Growth delay
  • Failure to thrive
  • Pain
  • Anemia
  • Visual impairment


SOURCES: OMIM MENDELIAN

More info about HYPERLIPOPROTEINEMIA, TYPE I

Top 5 symptoms//phenotypes associated to Anemia and Hyperhidrosis

Symptoms // Phenotype % cases
Splenomegaly Uncommon - Between 30% and 50% cases
Muscle weakness Uncommon - Between 30% and 50% cases
Fever Uncommon - Between 30% and 50% cases
Diarrhea Uncommon - Between 30% and 50% cases
Abdominal pain Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Hepatosplenomegaly Depressivity Hypertension Arthralgia Arrhythmia Abdominal distention Intestinal bleeding Subcutaneous nodule Skin rash Carcinoma Pain Growth delay Nausea and vomiting Seizures Weight loss Anxiety

Rare Symptoms - Less than 30% cases


Hypertensive crisis Areflexia Gastrointestinal infarctions Intussusception Failure to thrive Respiratory insufficiency Memory impairment Arthritis Hemolytic anemia Insomnia Hyperlipidemia Acanthocytosis Hallucinations Tachycardia Psoriasiform dermatitis Rectal prolapse Nausea Dilatation Paresthesia Myalgia Elevated hepatic transaminase Retinopathy Intellectual disability, mild Behavioral abnormality Anorexia Vomiting Dementia Edema Abnormality of the mouth Microcytic anemia Clubbing of fingers Hepatomegaly Visual impairment Hemangioma Fatigue Neoplasm Constipation Hypermelanotic macule Nevus Congestive heart failure Iron deficiency anemia Lymphadenopathy Renal cell carcinoma Skeletal muscle atrophy Elevated serum creatine phosphokinase Babinski sign Parkinsonism Sensory neuropathy Dyspnea Dyskinesia Confusion Rigidity Precocious puberty with Sertoli cell tumor Lower limb muscle weakness Clear cell renal cell carcinoma Endolymphatic sac tumor Mental deterioration Abnormality of vitamin metabolism Abnormality of movement Abnormality of the cerebral white matter Congenital shortened small intestine Thyroid nodule Uterine neoplasm Gastrointestinal carcinoma Dilated cardiomyopathy Dystonia Cerebral atrophy Arthrogryposis multiplex congenita Cardiomegaly Thick lower lip vermilion Abnormality of the face Lipodystrophy Hyperostosis Macroglossia Right bundle branch block Increased antibody level in blood Elevated erythrocyte sedimentation rate Lipoatrophy Episodic fever Erythema nodosum Arachnodactyly Clubbing of toes Macrotia Abnormality of the Leydig cells Short stature Cognitive impairment Abnormal pyramidal sign Peripheral neuropathy Dysarthria Gait disturbance Dysphagia Joint stiffness Cardiomyopathy Myopathy Hypertonia Prominent nose Chorea Personality changes Neuronal loss in central nervous system Recurrent pancreatitis Pancreatitis Hypertriglyceridemia Hepatic steatosis Pallor Irritability Jaundice Abnormality of the astrocytes Hypercholesterolemia Hyporeflexia of upper limbs Abnormal facial expression Blood group antigen abnormality Recurrent singultus Lipemia retinalis Abnormal corpus striatum morphology Atherosclerosis EMG: myopathic abnormalities Caudate atrophy Impaired proprioception Acute pancreatitis Chills Hyperlipoproteinemia Hypocholesterolemia Precocious atherosclerosis Foam cells Peritonitis Back pain Chronic pancreatitis Peripheral arterial stenosis Episodic abdominal pain Eruptive xanthomas Steatorrhea Glucose intolerance Increased circulating chylomicron concentration Abnormal lactate dehydrogenase activity Generalized-onset seizure Obsessive-compulsive behavior Rhabdomyolysis Bowel incontinence Sensory axonal neuropathy Ventricular fibrillation Emotional lability Hypersplenism Ventricular arrhythmia Pancreatic calcification Sleep apnea Cardiac arrest Sensorimotor neuropathy Left ventricular hypertrophy Involuntary movements Atrial fibrillation Increased hepatocellular lipid droplets Testicular neoplasm Abnormal social behavior Orofacial dyskinesia Impaired temperature sensation Generalized limb muscle atrophy Personality disorder Increased muscle fatiguability Hyporeflexia of lower limbs Excessive salivation Tics Impaired vibration sensation in the lower limbs Supraventricular tachycardia Motor axonal neuropathy Left bundle branch block Ventricular extrasystoles Bipolar affective disorder Restlessness Impaired pain sensation Intestinal polyp Red urine Bloody diarrhea Uveitis Cerebellar medulloblastoma Chronic disseminated intravascular coagulation Hyperkeratosis Photophobia Autoimmunity Papule Dry skin Epidermal acanthosis Chronic diarrhea Keratitis Atrophic scars Autoimmune hemolytic anemia Thyroiditis Keratoconjunctivitis sicca Antinuclear antibody positivity Venous malformation Follicular hyperkeratosis Villous atrophy Corneal neovascularization Increased IgA level Polyarticular arthritis Comedo Punctate keratitis Hypertrophic cardiomyopathy Neurological speech impairment Chest pain Migraine Pulmonary arterial hypertension Myocardial infarction Skin ulcer Multiple enchondromatosis Melena Aortic regurgitation Posterior uveitis Neutropenia Abnormal bleeding Abnormality of the cardiovascular system Recurrent pneumonia Alzheimer disease Body odor Fish odor Trimethylaminuria Recurrent respiratory infections Abnormality of the thyroid gland Pulmonary infiltrates B-cell lymphoma Mediastinal lymphadenopathy Abnormal nasolacrimal system morphology Thrombocytopenia Cavernous hemangioma Abnormality of the liver Leukemia Gastrointestinal hemorrhage Bone pain Abnormality of coagulation Prolonged bleeding time Pathologic fracture Abnormality of the vasculature Abnormality of the respiratory system Arteriovenous malformation Volvulus Medulloblastoma Chronic lymphatic leukemia Visceral angiomatosis Vasculitis Abnormal heart valve morphology Thrombophlebitis Intestinal obstruction Psychotic episodes Respiratory paralysis Paralytic ileus Elevated urinary delta-aminolevulinic acid Acute episodes of neuropathic symptoms Headache Abnormality of the kidney Gynecomastia Accelerated skeletal maturation Breast carcinoma Growth abnormality Polycystic kidney dysplasia Melanocytic nevus Clubbing Macule Abnormal urinary color Hamartoma Ovarian neoplasm Abnormality of the ureter Vitiligo Neoplasm of the pancreas Multiple myeloma Ovarian cyst Intestinal polyposis Pancreatic cysts Biliary tract abnormality Nasal polyposis Neoplasm of the breast Hamartomatous polyposis Hematemesis Delirium Diaphragmatic paralysis Hemoptysis Renal insufficiency Gangrene Cerebral ischemia Reduced consciousness/confusion Abnormal aortic valve morphology Inflammatory abnormality of the eye Abnormal pattern of respiration Arterial stenosis Ascending tubular aorta aneurysm Abnormal endocardium morphology Amaurosis fugax Arteritis Increased inflammatory response Intellectual disability Global developmental delay Paralysis Urinary retention Cranial nerve paralysis Ileus Dysuria Hepatocellular carcinoma Agitation Apathy Hyponatremia Paraparesis Lethargy Cutaneous photosensitivity Psychosis Urinary incontinence Coma Nephropathy Stage 5 chronic kidney disease Lactescent serum



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Arthritis and Craniosynostosis, related diseases and genetic alterations Myopathy and Flat face, related diseases and genetic alterations Cardiomyopathy and Elevated serum creatine phosphokinase, related diseases and genetic alterations Hypertelorism and Delayed eruption of teeth, related diseases and genetic alterations Sensorineural hearing impairment and Corneal dystrophy, related diseases and genetic alterations

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