Hypertension, and Psychosis

Diseases related with Hypertension and Psychosis

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


Top matches:

Medium match PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2; PPNAD2


PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2; PPNAD2 Is also known as cushing syndrome, adrenal, due to ppnad2|pigmented micronodular adrenocortical disease, primary, 2

Related symptoms:

  • Hypertension
  • Kyphosis
  • Depressivity
  • Osteoporosis
  • Osteopenia


SOURCES: OMIM MENDELIAN

More info about PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 2; PPNAD2

Medium match PORPHYRIA DUE TO ALA DEHYDRATASE DEFICIENCY


Porphyria of doss or deficiency of delta-aminolevulinic acid dehydratase (DALAD) is an extremely rare form of acute hepatic porphyria (see this term) characterized by neuro-visceral attacks without cutaneous manifestations.

PORPHYRIA DUE TO ALA DEHYDRATASE DEFICIENCY Is also known as porphyria due to alad deficiency|doss porphyria|delta-aminolevulinate dehydratase deficiency|alad porphyria|porphyria, alad|porphyria of doss|alad deficiency|porphyria due to delta-aminolevulinate dehydratase deficiency|porphobilinogen synthase deficiency

Related symptoms:

  • Seizures
  • Generalized hypotonia
  • Failure to thrive
  • Muscular hypotonia
  • Pain


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about PORPHYRIA DUE TO ALA DEHYDRATASE DEFICIENCY

Medium match PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1; PPNAD1


Primary pigmented micronodular adrenocortical disease is a form of ACTH-independent adrenal hyperplasia resulting in Cushing syndrome. It is usually seen as a manifestation of the Carney complex (CNC1 ), a multiple neoplasia syndrome. However, PPNAD can also occur in isolation (Groussin et al., 2002). Genetic Heterogeneity of Primary Pigmented Micronodular Adrenocortical DiseaseSee also PPNAD2 (OMIM ), caused by mutation in the PDE11A gene (OMIM ) on chromosome 2q31; PPNAD3 (OMIM ), caused by mutation in the PDE8B gene (OMIM ) on chromosome 5q13; and PPNAD4 (OMIM ), caused by a duplication on chromosome 19p13 that includes the PRKACA gene (OMIM ).

PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1; PPNAD1 Is also known as pigmented micronodular adrenocortical disease, primary, 1|cushing syndrome, adrenal, due to ppnad1|adrenocortical nodular dysplasia, primary

Related symptoms:

  • Neoplasm
  • Hypertension
  • Kyphosis
  • Obesity
  • Depressivity


SOURCES: OMIM MENDELIAN

More info about PIGMENTED NODULAR ADRENOCORTICAL DISEASE, PRIMARY, 1; PPNAD1

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Other less relevant matches:

Medium 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

Medium match HEREDITARY COPROPORPHYRIA


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

Medium match PORPHYRIA VARIEGATA


Variegate porphyria is a form of acute hepatic porphyria (see this term) characterized by the occurrence of neuro-visceral attacks with or without the presence of cutaneous lesions.

PORPHYRIA VARIEGATA Is also known as variegate porphyria|ppox deficiency|porphyria, south african type|protoporphyrinogen oxidase deficiency|vp

Related symptoms:

  • Intellectual disability
  • Seizures
  • Short stature
  • Growth delay
  • Nystagmus


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about PORPHYRIA VARIEGATA

Medium match GLYCOGEN STORAGE DISEASE DUE TO LAMP-2 DEFICIENCY


Glycogen storage disease due to LAMP-2 (Lysosomal-Associated Membrane Protein 2) deficiency is a lysosomal glycogen storage disease characterised by severe cardiomyopathy and variable degrees of muscle weakness, frequently associated with intellectual deficit.

GLYCOGEN STORAGE DISEASE DUE TO LAMP-2 DEFICIENCY Is also known as vacuolar cardiomyopathy and myopathy, x-linked|antopol disease|gsd due to lamp-2 deficiency|lysosomal glycogen storage disease without acid maltase deficiency, formerly|glycogenosis due to lamp-2 deficiency|gsd2b, formerly|gsd iib, formerly|glycogen stora

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Muscle weakness
  • Pain
  • Cognitive impairment


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about GLYCOGEN STORAGE DISEASE DUE TO LAMP-2 DEFICIENCY

Medium match CUSHING SYNDROME DUE TO MACRONODULAR ADRENAL HYPERPLASIA


ACTH-independent macronodular adrenal hyperplasia (AIMAH) is a rare cause of Cushing syndrome (CS; see this term) characterized by nodular enlargement of both adrenal glands (multiple nodules above 1 cm in diameter) that produce excess cortisol and features of adrenocorticotropic hormone (ACTH) independent CS (see this term).

CUSHING SYNDROME DUE TO MACRONODULAR ADRENAL HYPERPLASIA Is also known as cushing disease, pituitary|primary bilateral macronodular adrenal hyperplasia

Related symptoms:

  • Neoplasm
  • Failure to thrive
  • Muscle weakness
  • Hypertension
  • Skeletal muscle atrophy


SOURCES: ORPHANET OMIM MENDELIAN

More info about CUSHING SYNDROME DUE TO MACRONODULAR ADRENAL HYPERPLASIA

Medium match CUSHING DISEASE


Cushing disease (CD) is the most common cause of endogenous Cushing syndrome (CS; see this term) and is due to pituitary chronic over-secretion of ACTH by a pituitary corticotroph adenoma.

CUSHING DISEASE Is also known as corticotroph pituitary adenoma|pituitary-dependent cushing syndrome|pituitary corticotroph micro-adenoma

Related symptoms:

  • Failure to thrive
  • Cataract
  • Visual impairment
  • Hypertension
  • Fatigue


SOURCES: ORPHANET MENDELIAN

More info about CUSHING DISEASE

Medium match BILATERAL STRIOPALLIDODENTATE CALCINOSIS


Bilateral striopallidodentate calcinosis (BSPDC, also erroneously called Fahr disease) is characterized by the accumulation of calcium deposits in different brain regions, particularly the basal ganglia and dentate nucleus, and is often associated with neurodegeneration.

BILATERAL STRIOPALLIDODENTATE CALCINOSIS Is also known as cerebrovascular ferrocalcinosis|primary familial brain calcification|ferrocalcinosis, cerebrovascular|pfbc|bspdc|striopallidodentate calcinosis, bilateral|cerebral calcification, nonarteriosclerotic, idiopathic, adult-onset|basal ganglia calcification, id

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Microcephaly
  • Ataxia


SOURCES: ORPHANET OMIM MENDELIAN

More info about BILATERAL STRIOPALLIDODENTATE CALCINOSIS

Top 5 symptoms//phenotypes associated to Hypertension and Psychosis

Symptoms // Phenotype % cases
Depressivity Very Common - Between 80% and 100% cases
Anxiety Common - Between 50% and 80% cases
Thin skin Common - Between 50% and 80% cases
Pain Common - Between 50% and 80% cases
Seizures Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Abdominal pain Muscle weakness Diarrhea Intellectual disability Vomiting Tachycardia Truncal obesity Paralysis Constipation Agitation Round face Bruising susceptibility Mental deterioration Osteoporosis Fatigue Respiratory paralysis Kyphosis Neoplasm Arrhythmia Carcinoma Hypertrichosis Hepatomegaly Global developmental delay Insomnia Hallucinations Nausea and vomiting Cutaneous photosensitivity Hyponatremia Paresthesia Nausea Anemia Osteopenia Striae distensae Increased circulating cortisol level Behavioral abnormality Adrenal hyperplasia Mood changes Failure to thrive Peripheral neuropathy

Rare Symptoms - Less than 30% cases


Delirium Cognitive impairment Ileus Hepatocellular carcinoma Visual impairment Hyperlipidemia Pituitary adenoma Red urine Cardiomyopathy Bipolar affective disorder Skeletal muscle atrophy Myopathy Gait disturbance Confusion Headache Scarring Abnormal blistering of the skin Abnormality of the liver Fragile skin Urinary incontinence Visual hallucinations Visual loss Acute episodes of neuropathic symptoms Lethargy Abdominal colic Acne Moon facies Generalized hirsutism Diabetes mellitus Hypokalemia Hemolytic anemia Respiratory insufficiency Emotional lability Nephrolithiasis Arthralgia Obesity Elevated urinary delta-aminolevulinic acid Hepatosplenomegaly Paradoxical increased cortisol secretion on dexamethasone suppression test Myalgia Primary hypercortisolism Pigmented micronodular adrenocortical disease Decreased circulating ACTH level Recurrent skin infections Amenorrhea Hirsutism Recurrent fractures Venous thrombosis Oligomenorrhea Lipodystrophy Premature ovarian insufficiency Menorrhagia Telangiectasia of the skin Alopecia Sleep disturbance Edema Aseptic necrosis Glycogen accumulation in muscle fiber lysosomes Increased cerebral lipofuscin Generalized hyperpigmentation Cataract Infertility Facial erythema Hyperparathyroidism Glucose intolerance Metrorrhagia Alkalosis Vertebral compression fractures Ecchymosis Poor wound healing Abdominal obesity Biconcave vertebral bodies Increased circulating ACTH level Immunodeficiency Abnormality of the menstrual cycle Peripheral edema Increased body weight Menometrorrhagia Adrenocorticotropic hormone excess Dorsocervical fat pad Macronodular adrenal hyperplasia Abnormal fear/anxiety-related behavior Psychotic mentation Meningioma Onychomycosis Bradykinesia Microcephaly Lewy bodies Broad-based gait Clumsiness Muscle stiffness Schizophrenia Slurred speech Dysdiadochokinesis Oral-pharyngeal dysphagia Athetosis Mask-like facies Abnormality of neuronal migration Basal ganglia calcification Progressive encephalopathy Frontotemporal dementia Abnormal lower motor neuron morphology Progressive neurologic deterioration Calcinosis Focal dystonia Orofacial dyskinesia Pseudohypoparathyroidism Alcoholism Mood swings Subcutaneous hemorrhage Limb dysmetria Focal motor seizures Micrographia Progressive choreoathetosis Pill-rolling tremor Calcification of the small brain vessels Choreoathetosis Abnormality of extrapyramidal motor function Ataxia Abnormal pyramidal sign Motor delay Hyperreflexia Dysarthria Intrauterine growth retardation Tremor Dysphagia Ventriculomegaly Dystonia Thrombocytopenia Encephalopathy Dementia Gait ataxia Rigidity Corneal opacity Macular hypopigmentation Neurological speech impairment Abnormality of movement Dysmetria Vertigo Dyskinesia Postural instability Abnormal cerebellum morphology Parkinsonism Gliosis Chorea Memory impairment Neuronal loss in central nervous system Cerebral calcification Suicidal ideation Limb muscle weakness Left ventricular systolic dysfunction Prolonged neonatal jaundice Abnormality of metabolism/homeostasis Areflexia Acidosis Jaundice Elevated hepatic transaminase Irritability Pruritus Metabolic acidosis Hypotension Hypermelanotic macule Orthostatic hypotension Auditory hallucinations Paralytic ileus Paranoia Congenital hemolytic anemia Compensated hemolytic anemia Short stature Growth delay Nystagmus Fever Abnormality of the skeletal system Clinodactyly Abnormality of the kidney Hypopigmentation of the skin Tetraplegia Splenomegaly Hypertensive crisis Hypopigmented skin patches Hyperhidrosis Generalized hypotonia Muscular hypotonia Sensory neuropathy Polyneuropathy Hemiparesis Motor axonal neuropathy Wrist drop Cerebral cortical atrophy Adrenocortical carcinoma Intellectual disability, mild Renal insufficiency Weight loss Psychotic episodes Stage 5 chronic kidney disease Nephropathy Coma Abdominal distention Anorexia Paraparesis Cranial nerve paralysis Apathy Dysuria Urinary retention Diaphragmatic paralysis Abnormal urinary color Aspiration Chronic kidney disease Myocardial necrosis Hypokinesia Exercise intolerance Ventricular tachycardia Respiratory insufficiency due to muscle weakness Cone/cone-rod dystrophy EMG: myopathic abnormalities Ventricular arrhythmia Abnormal electroretinogram Back pain Neurodevelopmental delay Generalized amyotrophy Abnormal retinal morphology Cardiorespiratory arrest Decreased liver function Abnormality of the gastrointestinal tract Reduced ejection fraction Wolff-Parkinson-White syndrome Myocardial fibrosis Myofibrillar myopathy Skeletal myopathy Autophagic vacuoles Muscle flaccidity Retinal pigment epithelial mottling Exercise-induced muscle cramps Impaired myocardial contractility Ventricular preexcitation Cardiac arrest Left ventricular hypertrophy Milia Reduced visual acuity Restlessness Neoplasm of the liver Motor polyneuropathy Dark urine Premature adrenarche Porphyrinuria Myopia Respiratory distress Congestive heart failure Elevated serum creatine phosphokinase Pes cavus Hyperactivity Proximal muscle weakness Palpitations Hypertrophic cardiomyopathy Abnormality of the eye Retinopathy Dilated cardiomyopathy Distal amyotrophy Distal sensory impairment Chest pain Progressive visual loss Pigmentary retinopathy Cardiomegaly Ventricular hypertrophy Atrial fibrillation Dense calcifications in the cerebellar dentate nucleus



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