Hypertension, and Aggressive behavior

Diseases related with Hypertension and Aggressive behavior

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


Top matches:

Medium match NEONATAL GLYCINE ENCEPHALOPATHY


Neonatal glycine encephalopathy is a frequent, usually severe form of glycine encephalopathy (GE; see this term) characterized by coma, apnea, hypotonia, seizure and myoclonic jerks in the neonatal period, and subsequent developmental delay.

NEONATAL GLYCINE ENCEPHALOPATHY Is also known as classic glycine encephalopathy|neonatal nkh|nkh|neonatal non-ketotic hyperglycinemia|hyperglycinemia, nonketotic

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about NEONATAL GLYCINE ENCEPHALOPATHY

Medium match FRAGILE X-ASSOCIATED TREMOR/ATAXIA SYNDROME


Fragile X-associated tremor/ataxia syndrome (FXTAS) is a rare neurodegenerative disorder characterized by adult-onset progressive intention tremor and gait ataxia.

FRAGILE X-ASSOCIATED TREMOR/ATAXIA SYNDROME Is also known as fxtas syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Hearing impairment
  • Ataxia


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about FRAGILE X-ASSOCIATED TREMOR/ATAXIA SYNDROME

Medium match RIBOFLAVIN TRANSPORTER DEFICIENCY


Riboflavin transporter deficiency (RTD) is a progressive motor neuron disorder characterized by respiratory insufficiency, sensorineural deafness and progressive ponto-bulbar palsy.

RIBOFLAVIN TRANSPORTER DEFICIENCY Is also known as sensorineural hearing loss-pontobulbar palsy syndrome|brown-vialetto-van laere syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Ataxia
  • Muscle weakness
  • Muscular hypotonia


SOURCES: ORPHANET MENDELIAN

More info about RIBOFLAVIN TRANSPORTER DEFICIENCY

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Other less relevant matches:

Medium match JUVENILE HUNTINGTON DISEASE


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

Medium match 3Q29 MICRODELETION SYNDROME


3q29 microdeletion syndrome is a recurrent subtelomeric deletion syndrome with variable clinical manifestations including intellectual deficit and dysmorphic features.

3Q29 MICRODELETION SYNDROME Is also known as del(3)(q29)|microdeletion 3q29 syndrome|3q subtelomere deletion syndrome|monosomy 3q29|monosomy 3qter|3qter deletion

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Microcephaly
  • Ataxia
  • Failure to thrive


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about 3Q29 MICRODELETION SYNDROME

Medium match FEINGOLD SYNDROME 1; FGLDS1


Feingold syndrome is an autosomal dominant disorder characterized by variable combinations of microcephaly, limb malformations, esophageal and duodenal atresias, and learning disability/mental retardation. Hand and foot abnormalities may include hypoplastic thumbs, clinodactyly of second and fifth fingers, syndactyly (characteristically between second and third and fourth and fifth toes), and shortened or absent middle phalanges. Cardiac and renal malformations, vertebral anomalies, and deafness have also been described in a minority of patients (summary by Teszas et al., 2006). Genetic Heterogeneity of Feingold SyndromeFeingold syndrome-2 (FGLDS2 ) is caused by hemizygous deletion of the MIR17HG gene (OMIM ) on chromosome 13q31.3.

FEINGOLD SYNDROME 1; FGLDS1 Is also known as digital anomalies with short palpebral fissures and atresia of esophagus or duodenum|microcephaly, mental retardation, and tracheoesophageal fistula syndrome|oded syndrome|mmt syndrome|oculodigitoesophagoduodenal syndrome|moded|feingold syndrome|microceph

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Hearing impairment


SOURCES: ORPHANET OMIM MENDELIAN

More info about FEINGOLD SYNDROME 1; FGLDS1

Medium match 17Q23.1Q23.2 MICRODELETION SYNDROME


17q23.1q23.2 microdeletion syndrome is a recently described syndrome characterized by developmental delay, microcephaly, short stature, heart defects and limb abnormalities.

17Q23.1Q23.2 MICRODELETION SYNDROME Is also known as 17q23.1-q23.2 microdeletion syndrome|del(17)(q23.1q23.2)|monosomy 17q23.1q23.2|monosomy 17q23.1-q23.2

Related symptoms:

  • Global developmental delay
  • Short stature
  • Hearing impairment
  • Microcephaly
  • Scoliosis


SOURCES: ORPHANET OMIM MENDELIAN

More info about 17Q23.1Q23.2 MICRODELETION SYNDROME

Medium match GAUCHER DISEASE TYPE 3


Gaucher disease type 3 is the subacute neurological form of Gaucher disease (GD; see this term) characterized by progressive encephalopathy and associated with the systemic manifestations (organomegaly, bone involvement, cytopenia) of GD type 1 (see this term).

GAUCHER DISEASE TYPE 3 Is also known as chronic neuronopathic gaucher disease|cerebral juvenile and adult form of gaucher disease|gaucher disease, subacute neuronopathic type

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Scoliosis


SOURCES: ORPHANET MENDELIAN

More info about GAUCHER DISEASE TYPE 3

Medium match FLOATING-HARBOR SYNDROME


Floating-Harbor syndrome is a genetic developmental disorder characterized by facial dysmorphism, short stature with delayed bone age, and expressive language delay.

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Hearing impairment


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about FLOATING-HARBOR SYNDROME

Medium match CORNELIA DE LANGE SYNDROME 1; CDLS1


The Cornelia de Lange syndrome (CDLS) is a multisystem malformation syndrome recognized primarily on the basis of characteristic facial dysmorphism, including low anterior hairline, arched eyebrows, synophrys, anteverted nares, maxillary prognathism, long philtrum, thin lips, and 'carp' mouth, in association with prenatal and postnatal growth retardation, mental retardation and, in many cases, upper limb anomalies. However, there is wide clinical variability in this disorder, with milder phenotypes that may be difficult to ascertain on the basis of physical features (summary by Rohatgi et al., 2010).Boyle et al. (2015) provided a detailed review of CDLS, including clinical features, diagnosis, and genetic counseling. Genetic Heterogeneity of Cornelia de Lange SyndromeAbout 50 to 60% of the cases of CDLS are due to mutation in the NIPBL gene (Musio et al., 2006; Rohatgi et al., 2010).One X-linked form of CDLS (CDLS2 ) is caused by mutation in the SMC1A gene (OMIM ), which accounts for about 5% of cases. Two milder variants of Cornelia de Lange syndrome have been identified: CDLS3 (OMIM ), caused by mutation in the SMC3 gene (OMIM ), and CDLS4 (OMIM ), caused by mutation in the RAD21 gene (OMIM ). All 4 genes, NIPBL, SMC1A, SMC3, and RAD21, encode components of the cohesin complex. Another X-linked form, CDLS5 (OMIM ), is caused by mutation in the HDAC8 gene (OMIM ), the vertebrate histone deacetylase of SMC3.

CORNELIA DE LANGE SYNDROME 1; CDLS1 Is also known as typus degenerativus amstelodamensis|brachmann-de lange syndrome|cdl|de lange syndrome|cdls|bdls

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Short stature
  • Generalized hypotonia


SOURCES: OMIM MENDELIAN

More info about CORNELIA DE LANGE SYNDROME 1; CDLS1

Top 5 symptoms//phenotypes associated to Hypertension and Aggressive behavior

Symptoms // Phenotype % cases
Intellectual disability Common - Between 50% and 80% cases
Global developmental delay Common - Between 50% and 80% cases
Seizures Common - Between 50% and 80% cases
Microcephaly Common - Between 50% and 80% cases
Ataxia Common - Between 50% and 80% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Vomiting Hyperactivity Gait disturbance Clinodactyly of the 5th finger Delayed speech and language development Short stature Behavioral abnormality Cognitive impairment Hearing impairment Hyperreflexia Clinodactyly Strabismus Dysarthria Failure to thrive Tremor Micrognathia Gastroesophageal reflux Abnormal facial shape Dysphagia Depressivity Autism Low-set ears Growth delay Small for gestational age High palate Myoclonus Anxiety Long eyelashes Clubbing Atrial septal defect Scoliosis Pulmonary arterial hypertension Postnatal growth retardation Abnormality of eye movement Rigidity Anemia Progressive cerebellar ataxia Wide nasal bridge Mental deterioration Hypertelorism Dementia Gait ataxia Depressed nasal bridge Triangular face Nystagmus Epicanthus Patent ductus arteriosus Single transverse palmar crease Muscular hypotonia Hydrocephalus Intellectual disability, mild Thrombocytopenia Hyporeflexia Prominent nasal bridge Intellectual disability, moderate Irritability Thin upper lip vermilion Posteriorly rotated ears Inguinal hernia Intrauterine growth retardation Hypospadias Abnormality of the dentition Delayed skeletal maturation

Rare Symptoms - Less than 30% cases


Abnormal heart morphology Arthritis Abnormality of the hand Dystonia Frontal bossing Short middle phalanx of finger 2-3 toe syndactyly Bulbar palsy Oral cleft Mandibular prognathia Abnormality of digit Short neck Headache Finger clinodactyly Abnormality of the skeletal system Abnormality of the spleen Cryptorchidism Otitis media Neoplasm Ptosis Microdontia Everted lower lip vermilion Tapered finger Cleft palate Sandal gap Conductive hearing impairment Neurodegeneration Thin vermilion border Pulmonic stenosis Hirsutism Macrotia Hernia Joint laxity Low posterior hairline Aspiration Sensorineural hearing impairment Respiratory tract infection Downturned corners of mouth Short philtrum Brachydactyly Small hand Nasal speech Telecanthus Anteverted nares Syndactyly Upslanted palpebral fissure Toe syndactyly Incoordination Craniosynostosis Macrocephaly Short palpebral fissure Joint hyperflexibility Progressive neurologic deterioration Choanal atresia Short thumb Facial asymmetry Astrocytosis Talipes equinovarus Weak cry Bradykinesia Brain atrophy Abnormal cerebellum morphology Abnormality of the cerebral white matter Hypothyroidism Cerebral cortical atrophy Cerebellar atrophy Muscle weakness Myopia Opisthotonus Hypertonia Restlessness Impulsivity Abnormal autonomic nervous system physiology Leukopenia Limb ataxia Chorea Proteinuria Pallor Attention deficit hyperactivity disorder Autistic behavior Malabsorption Encephalopathy Intellectual disability, severe Optic atrophy Feeding difficulties Generalized hypotonia Intention tremor Abnormality of movement Prominent nose Bipolar affective disorder Bulbous nose Dyspnea Widely spaced teeth Highly arched eyebrow Narrow mouth Obsessive-compulsive behavior Oculomotor apraxia Increased susceptibility to fractures Dental malocclusion Hypoalbuminemia Abnormal saccadic eye movements Aortic valve calcification Broad nasal tip Cholelithiasis Mitral valve calcification Hypoplasia of the maxilla Portal hypertension Spontaneous hematomas Abnormal thrombosis Abnormality of the thorax Osteolysis Abnormality of the acoustic reflex Increased bone mineral density Pancytopenia Erlenmeyer flask deformity of the femurs Decreased beta-glucocerebrosidase protein and activity Syncope Hematological neoplasm Cyanosis Horizontal supranuclear gaze palsy Epistaxis Sleep myoclonus Cardiac valve calcification Decreased body weight Underdeveloped nasal alae Hydrops fetalis Bone pain Abnormality of ion homeostasis Lymphopenia Menorrhagia Abnormal myocardium morphology Pulmonary fibrosis Feeding difficulties in infancy Aseptic necrosis Restrictive deficit on pulmonary function testing Wide mouth Joint stiffness Hepatocellular carcinoma Kyphoscoliosis Thoracic kyphosis Slow saccadic eye movements Camptodactyly of finger Vertebral compression fractures Hydronephrosis Avascular necrosis of the capital femoral epiphysis Hypercoagulability Supranuclear gaze palsy Deeply set eye Multiple myeloma Abnormal heart valve morphology Exertional dyspnea Increased antibody level in blood Constipation Umbilical hernia Abnormality of cardiovascular system morphology Petechiae Restrictive ventilatory defect Interstitial pulmonary abnormality Pericardial effusion Babinski sign Generalized osteosclerosis Neurological speech impairment Abnormal retinal morphology Lower limb hyperreflexia Abnormality of the sternum Smooth philtrum Protein-losing enteropathy Orthopnea Poor speech Hypermetropia Dilatation Sprengel anomaly Hypoplasia of penis Elbow flexion contracture Limited elbow extension Ectopic kidney Cutis marmorata Tricuspid regurgitation Proximal placement of thumb Self-injurious behavior Pyloric stenosis Short metatarsal Deep philtrum Abnormality of the urinary system Hypoplasia of the radius Relative macrocephaly Torticollis Spontaneous abortion Increased body weight Hypoplastic nipples Low anterior hairline Recurrent urinary tract infections Hypertrichosis Renal hypoplasia Blue sclerae High myopia Congenital diaphragmatic hernia Webbed neck Vesicoureteral reflux Sepsis Renal cyst Microcornea Delayed eruption of teeth Sleep disturbance Dislocated radial head Oligodactyly Pulmonary hypoplasia Supernumerary ribs Hypoplastic radial head Abnormality of the umbilicus Reduced renal corticomedullary differentiation Otitis media with effusion Malrotation of colon Duplication of internal organs Projectile vomiting Left-to-right shunt Hypertropia Esophageal stenosis Hypoplastic male external genitalia Curly eyelashes Absent hand Gastroparesis Phocomelia Ectrodactyly Optic nerve coloboma Poor appetite Hiatus hernia Aspiration pneumonia Esophagitis Hypoplastic labia majora Abnormality of the gastrointestinal tract Thick upper lip vermilion Hand oligodactyly Recurrent hypoglycemia Volvulus Panhypopituitarism Peters anomaly Short sternum Perimembranous ventricular septal defect High, narrow palate Thick eyebrow Coarctation of aorta Lipoma Spinal dysraphism Stiff neck Tethered cord Broad columella Hyperextensibility of the finger joints Speech apraxia Enlarged joints 11 pairs of ribs Villous atrophy Enuresis Short attention span Abnormality of the clavicle Short columella Cone-shaped epiphyses of the phalanges of the hand Generalized myoclonic seizures Expressive language delay Abnormality of the fingernails Apraxia Interphalangeal joint contracture of finger Recurrent otitis media Broad thumb Generalized hirsutism Nephrocalcinosis Abnormality of the voice Short clavicles Trigonocephaly Language impairment Preauricular pit High pitched voice Celiac disease Proportionate short stature Short upper lip Varicocele Cleft upper lip Prominent forehead Vertigo Astigmatism Micromelia Synophrys Hip dislocation Abnormality of the pinna Camptodactyly Hypertrophic cardiomyopathy Hypoglycemia Retrognathia Proptosis Glaucoma Brachycephaly Hyperhidrosis Severe short stature Persistent left superior vena cava Broad fingertip Pseudoarthrosis Congenital pseudoarthrosis of the clavicle Congenital posterior urethral valve Epididymal cyst Enlarged naris Curved fingers Abnormal soft palate morphology Pneumonia Generalized cerebral atrophy/hypoplasia Mesocardia Fever Ventricular septal defect Cardiomyopathy Long philtrum Abnormal bleeding 4-5 toe syndactyly Abdominal distention Inertia Gynecomastia Hallucinations Optic disc pallor Limb muscle weakness Facial palsy Hypogonadism Respiratory insufficiency Skeletal muscle atrophy Visual impairment Impaired tandem gait Subcortical dementia Retrocollis Progressive hearing impairment Obsessive-compulsive trait Diffuse cerebellar atrophy Impaired distal vibration sensation Abnormal nerve conduction velocity Abnormality of brainstem morphology Pollakisuria Poor fine motor coordination Saccadic smooth pursuit Dysesthesia Kinetic tremor Disinhibition Olivopontocerebellar atrophy Cranial nerve paralysis Sleep apnea Action tremor Generalized-onset seizure Hypokinesia Akinesia Personality changes Rheumatoid arthritis Slurred speech Hyperkinesis Schizophrenia Involuntary movements Clumsiness Broad-based gait Type II diabetes mellitus Neuronal loss in central nervous system Cachexia Gliosis Falls Infertility Cough Weight loss Diabetes mellitus Ventriculomegaly Abnormality of macular pigmentation Abnormal cranial nerve morphology Iris hypopigmentation Abnormality of color vision Diabetes insipidus Diffuse cerebral atrophy Urinary bladder sphincter dysfunction Bronchitis Intellectual disability, profound Delirium Posterior fossa cyst Hyperglycinuria Vertical supranuclear gaze palsy Hyperglycinemia Ketoacidosis Infantile spasms Spastic diplegia Poor suck Choreoathetosis Hypsarrhythmia Aciduria Episodic ketoacidosis Coma Neutropenia Lethargy Severe global developmental delay Apnea Abnormality of the nervous system Neonatal hypotonia Acidosis Agenesis of corpus callosum Visual loss Hypoplasia of the corpus callosum Motor delay Nonketotic hyperglycinemia Recurrent singultus Atrophy/Degeneration affecting the brainstem Paraparesis Resting tremor Abnormality of the thyroid gland Bowel incontinence Global brain atrophy Agitation Impotence Mask-like facies Postural tremor Apathy Premature ovarian insufficiency Dysdiadochokinesis Spastic paraparesis Horizontal nystagmus Pill-rolling tremor Memory impairment Hypotension Urinary incontinence Parkinsonism Postural instability Distal sensory impairment Dysmetria Stroke Myalgia Proximal muscle weakness Peripheral neuropathy Pain Muscle fibrillation Cerebellar vermis atrophy Ascites Esotropia Mild global developmental delay Blepharitis Shawl scrotum Slender finger Long fingers Chronic otitis media Congenital contracture Bicuspid aortic valve Sacral dimple Bilateral single transverse palmar creases Abnormality of epiphysis morphology Limitation of joint mobility Patellar hypoplasia Arachnodactyly Retinopathy Abnormal cardiac septum morphology Protruding ear Pes planus Malar flattening Deviation of the 2nd finger Aplasia/Hypoplasia of the middle phalanx of the 5th finger Aplasia/Hypoplasia of the middle phalanx of the 2nd finger Small anterior fontanelle Annular pancreas Aplasia of the middle phalanx of the hand Bifid nose Moderate global developmental delay Accessory spleen Osteoporosis Hematuria Cirrhosis Lymphadenopathy Delayed puberty Ophthalmoplegia Generalized tonic-clonic seizures Corneal opacity Abnormal pyramidal sign Difficulty walking Hepatosplenomegaly Osteopenia Abdominal pain Recurrent respiratory infections Long toe Arrhythmia Kyphosis Splenomegaly Congestive heart failure Diarrhea Edema Fatigue Hepatomegaly Chalazion Coxa magna Retinopathy of prematurity Shallow acetabular fossae Frontal balding Intestinal atresia Upper limb undergrowth Short nose Aortic valve stenosis Anorexia Stereotypy Dental crowding Psychosis Long face Abnormality of skin pigmentation Pectus carinatum Cleft lip Pectus excavatum Microphthalmia Downslanted palpebral fissures Horseshoe kidney Cataract Oral motor hypotonia Frequent temper tantrums Suicidal ideation Neuronal loss in basal ganglia Abnormal involuntary eye movements Mania Paranoia Testicular atrophy Dilated fourth ventricle Chronic bronchitis Head tremor Narrow face Shallow orbits Periorbital fullness Narrow palpebral fissure Duodenal atresia Asplenia Polysplenia Short 5th finger Depressed nasal tip Vocal cord paralysis External ear malformation Esophageal atresia Prominent occiput Hallux valgus Tracheoesophageal fistula Nephritis Short toe Broad face Abnormal vertebral morphology Abnormal form of the vertebral bodies Decreased fetal movement Specific learning disability Thick vermilion border Anal atresia Finger syndactyly Blepharophimosis Polyhydramnios Renal insufficiency Six lumbar vertebrae Subvalvular aortic stenosis Dysplastic tricuspid valve



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Intrauterine growth retardation and Optic disc pallor, related diseases and genetic alterations Congestive heart failure and Hypermetropia, related diseases and genetic alterations Optic atrophy and Limb undergrowth, related diseases and genetic alterations Delayed speech and language development and Round face, related diseases and genetic alterations Failure to thrive and Gastroesophageal reflux, related diseases and genetic alterations

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