Hypertension, and Hyperhidrosis

Diseases related with Hypertension and Hyperhidrosis

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

Top matches:

Related symptoms:

  • Neoplasm
  • Hypertension
  • Hyperhidrosis
  • Vertigo
  • Tachycardia


SOURCES: OMIM MENDELIAN

More info about PARAGANGLIOMAS 5; PGL5

PARAGANGLIOMAS 3; PGL3 Is also known as glomus tumors, familial, 3

Related symptoms:

  • Hyperhidrosis
  • Tachycardia
  • Palpitations
  • Hoarse voice
  • Cranial nerve paralysis


SOURCES: OMIM MENDELIAN

More info about PARAGANGLIOMAS 3; PGL3

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

Other less relevant matches:

PARAGANGLIOMAS 4; PGL4 Is also known as paraganglioma, familial malignant|pheochromocytoma, extraadrenal, and cervical paraganglioma|carotid body tumors and multiple extraadrenal pheochromocytomas|pheochromocytoma, familial extraadrenal|paragangliomas, hereditary extraadrenal

Related symptoms:

  • Neoplasm
  • Pain
  • Hypertension
  • Congestive heart failure
  • Headache


SOURCES: OMIM MENDELIAN

More info about PARAGANGLIOMAS 4; PGL4

NEDIM is a neurodevelopmental and neurodegenerative disorder characterized by delayed psychomotor development and infantile or childhood onset of hyperkinetic involuntary movements, including chorea and athetosis. The abnormal movements can be severe, sometimes resulting in inability to sit, walk, speak, or eat. Hyperkinetic movements can be exacerbated by specific triggers, such as stress, illness, or high temperature. Some patients have brain abnormalities, such as cerebral atrophy or thin corpus callosum, and some patients may develop seizures (summary by Ananth et al., 2016 and Danti et al., 2017).

Related symptoms:

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


SOURCES: OMIM MENDELIAN

More info about NEURODEVELOPMENTAL DISORDER WITH INVOLUNTARY MOVEMENTS; NEDIM

Hypotrichosis - lymphedema - telangiectasia is an extremely rare syndromic lymphedema disorder characterized by early-onset hypotrichosis, childhood-onset lymphedema, and variable telangiectasia, particularly of the palms.

HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME Is also known as hypotrichosis-lymphedema-telangiectasia-membranoproliferative glomerulonephritis syndrome

Related symptoms:

  • Hypertension
  • Respiratory distress
  • Abnormality of the dentition
  • Alopecia
  • Hyperhidrosis


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about HYPOTRICHOSIS-LYMPHEDEMA-TELANGIECTASIA-RENAL DEFECT SYNDROME

Paragangliomas, also referred to as 'glomus body tumors,' are tumors derived from paraganglia located throughout the body. Nonchromaffin types primarily serve as chemoreceptors (hence, the tumor name 'chemodectomas') and are located in the head and neck region (i.e., carotid body, jugular, vagal, and tympanic regions), whereas chromaffin types have endocrine activity, conventionally referred to as 'pheochromocytomas,' and are usually located below the head and neck (i.e., adrenal medulla and pre- and paravertebral thoracoabdominal regions). PGL can manifest as nonchromaffin head and neck tumors only, adrenal and/or extraadrenal pheochromocytomas only, or a combination of the 2 types of tumors (Baysal, 2002; Neumann et al., 2004).The triad of gastric leiomyosarcoma, pulmonary chondroma, and extraadrenal paraganglioma constitutes a syndrome that occurs mainly in young women and is known as the Carney triad (OMIM ). This triad is not to be confused with the other Carney syndrome of myxoma, spotty pigmentation, and endocrinopathy (OMIM ).Baysal (2008) provided a review of the molecular pathogenesis of hereditary paraganglioma. Genetic Heterogeneity of ParagangliomasSee also PGL4 (OMIM ), caused by mutation in the SDHB gene (OMIM ) on chromosome 1p36; PGL3 (OMIM ), caused by mutation in the SDHC gene (OMIM ) on chromosome 1q21; PGL2 (OMIM ), caused by mutation in the SDHAF2 gene (OMIM ) on chromosome 11q13; and PGL5 (OMIM ), caused by mutation in the SDHA gene (OMIM ) on chromosome 5p15.

PARAGANGLIOMAS 1; PGL1 Is also known as paraganglioma, carotid body|glomus tumors, familial, 1|cbt1|glomus jugulare tumors|paragangliomas, familial, 1|chemodectomas|paragangliomas, familial nonchromaffin, 1|carotid body tumors|pgl|paragangliomata

Related symptoms:

  • Neoplasm
  • Pain
  • Hypertension
  • Hyperhidrosis
  • Dyspnea


SOURCES: OMIM MENDELIAN

More info about PARAGANGLIOMAS 1; PGL1

Some ectodermal dysplasias are here classified as congenital disorders characterized by abnormal development in 2 or more ectodermal structures (hair, nails, teeth, and sweat glands) without other systemic findings.Hypohidrotic, or anhidrotic, ectodermal dysplasia is characterized by a triad of signs comprising sparse hair (hypotrichosis), abnormal or missing teeth (anodontia or hypodontia), and inability to sweat (anhidrosis or hypohidrosis). Typical clinical manifestations also include dryness of the skin, eyes, airways, and mucous membranes presumably due to the defective development of several exocrine glands. Hypohidrotic ectodermal dysplasia can be associated with dysmorphic features (forehead bumps, rings under the eyes, everted nose, and prominent lips) and occasionally with absent nipples (summary by Cluzeau et al., 2011).For a discussion of genetic heterogeneity of hypohidrotic/anhidrotic ectodermal dysplasia, see {305100}.

ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B Is also known as eda|ectodermal dysplasia, hypohidrotic|hed|ectodermal dysplasia, anhidrotic

Related symptoms:

  • Depressed nasal bridge
  • Hypertension
  • Frontal bossing
  • Hyperhidrosis
  • Hyperkeratosis


SOURCES: OMIM MENDELIAN

More info about ECTODERMAL DYSPLASIA 10B, HYPOHIDROTIC/HAIR/TOOTH TYPE, AUTOSOMAL RECESSIVE; ECTD10B

Adrenocortical carcinoma (ACC) is a cancer that arises from the adrenal cortex.

Related symptoms:

  • Neoplasm
  • Muscle weakness
  • Pain
  • Hypertension
  • Abnormality of metabolism/homeostasis


SOURCES: OMIM ORPHANET MENDELIAN

More info about ADRENOCORTICAL CARCINOMA

Fatal familial insomnia (FFI) is a very rare form of prion disease (see this term) characterized by subacute onset of insomnia showing as a reduced overall sleep time, autonomic dysfunction, and motor disturbances.

FATAL FAMILIAL INSOMNIA Is also known as insomnia, fatal familial

Related symptoms:

  • Seizures
  • Ataxia
  • Nystagmus
  • Spasticity
  • Hypertension


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about FATAL FAMILIAL INSOMNIA

Top 5 symptoms//phenotypes associated to Hypertension and Hyperhidrosis

Symptoms // Phenotype % cases
Tachycardia Common - Between 50% and 80% cases
Neoplasm Uncommon - Between 30% and 50% cases
Anxiety Uncommon - Between 30% and 50% cases
Paraganglioma Uncommon - Between 30% and 50% cases
Palpitations Uncommon - Between 30% and 50% cases

Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases

Episodic paroxysmal anxiety Glomus jugular tumor Extraadrenal pheochromocytoma Pain Hypertension associated with pheochromocytoma Chemodectoma Pulsatile tinnitus Pheochromocytoma Recurrent paroxysmal headache Cranial nerve paralysis Hoarse voice Adrenal pheochromocytoma

Rare Symptoms - Less than 30% cases

Hypotrichosis Seizures Spasticity Fever Cerebellar atrophy Sparse body hair Weight loss Encephalopathy Myoclonus Absent eyebrow Thin skin Hyperkinesis Carcinoma Sparse hair Vocal cord paralysis Depressivity Loss of voice Elevated circulating catecholamine level Hypoplastic nipples Increased circulating cortisol level Increased body weight Sparse and thin eyebrow Hypohidrosis Hypokalemia Striae distensae Adrenocorticotropic hormone deficiency Hyperaldosteronism Irritability Pollakisuria Adrenocortical carcinoma Lung adenocarcinoma Increased urinary cortisol level Panic attack Depressed nasal ridge Hypertrichosis Type I diabetes mellitus Soft skin Anhidrosis Anodontia Agenesis of permanent teeth Heat intolerance Increased circulating androgen level Aplasia/Hypoplasia of the eyebrow Absent nipple Anhidrotic ectodermal dysplasia Hypohidrotic ectodermal dysplasia Everted upper lip vermilion Sparse eyelashes Periorbital wrinkles Periorbital hyperpigmentation Palmoplantar hyperkeratosis Muscle weakness Abnormality of metabolism/homeostasis Oligodontia Diabetes mellitus Abdominal pain Anterior hypopituitarism Dementia Abnormality of urine homeostasis Insomnia Diplopia Hallucinations Abnormal autonomic nervous system physiology Slurred speech Apathy Stridor Agitation Impotence Aphasia Hyperventilation Neuronal loss in central nervous system Urinary bladder sphincter dysfunction Hypothermia Bulbar signs Dysuria Central apnea Astrocytosis Urinary retention Hypersomnia Delirium Progressive neurologic deterioration Memory impairment Increased serum estradiol Fatigue Abnormality of reproductive system physiology Paradoxical increased cortisol secretion on dexamethasone suppression test Elevated serum 11-deoxycortisol Abnormal serum dehydroepiandrosterone level Increased serum androstenedione Ataxia Nystagmus Dysarthria Tremor Dysphagia Gliosis Constipation Ectodermal dysplasia Gait ataxia Apnea Mental deterioration Generalized tonic-clonic seizures Confusion Inability to walk Neurodegeneration Coma Microdontia Emphysema Hypodontia Abnormality of movement Motor delay Ventriculomegaly Hypoplasia of the corpus callosum Dystonia Renal insufficiency Cerebral atrophy Absent speech Elevated serum creatine phosphokinase Dyskinesia Microcephaly Tetraplegia Chorea Focal-onset seizure Choreoathetosis Involuntary movements Infantile muscular hypotonia Poor head control Focal impaired awareness seizure Cognitive impairment Generalized hypotonia Athetosis Body odor Vertigo Anemia Splenomegaly Neutropenia Abnormal bleeding Abnormality of the cardiovascular system Recurrent pneumonia Alzheimer disease Fish odor Global developmental delay Trimethylaminuria Congestive heart failure Headache Neuroblastoma Renal cell carcinoma Gastrointestinal stroma tumor Paraganglioma of head and neck Elevated urinary catecholamines Intellectual disability Self-injurious behavior Atrophy/Degeneration affecting the brainstem Delayed eruption of teeth Hypoplastic right heart Dyspnea Conductive hearing impairment Postural instability Dysphonia Neurofibromas Neoplasm of the lung Chronic obstructive pulmonary disease Leiomyosarcoma Vagal paraganglioma Palmar telangiectasia Glomus tympanicum paraganglioma Pulmonary chondroma Gastric leiomyosarcoma Depressed nasal bridge Frontal bossing Hyperkeratosis Short distal phalanx of finger Thick vermilion border Everted lower lip vermilion Plantar telangiectasia Predominantly lower limb lymphedema Respiratory distress Hydrops fetalis Abnormality of the dentition Alopecia Erythema Ascites Nevus Sparse scalp hair Telangiectasia Lymphedema Abnormality of the nail Abnormality of the lymphatic system Dermal atrophy Pleural effusion Cutis marmorata Palpebral edema Absent eyelashes Hydrocele testis Nonimmune hydrops fetalis Alopecia totalis Toenail dysplasia Snoring


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