Abnormal facial shape, and Coronary artery atherosclerosis

Diseases related with Abnormal facial shape and Coronary artery atherosclerosis

In the following list you will find some of the most common rare diseases related to Abnormal facial shape and Coronary artery atherosclerosis that can help you solving undiagnosed cases.


Top matches:

Low match AUTOSOMAL SEMI-DOMINANT SEVERE LIPODYSTROPHIC LAMINOPATHY


Related symptoms:

  • Micrognathia
  • Hepatomegaly
  • Myopathy
  • Congestive heart failure
  • Splenomegaly


SOURCES: ORPHANET MENDELIAN

More info about AUTOSOMAL SEMI-DOMINANT SEVERE LIPODYSTROPHIC LAMINOPATHY

Low match FAMILIAL PARTIAL LIPODYSTROPHY, DUNNIGAN TYPE


Familial Partial lipodystrophy, Dunnigan type (FPLD2) is a rare form of genetic lipodystrophy (see this term) characterized by a loss of subcutaneous adipose tissue from the trunk, buttocks and limbs; fat accumulation in the neck, face, axillary and pelvic regions; muscular hypertrophy; and usually associated with metabolic complications such as insulin resistance, diabetes mellitus, dyslipidemia and liver steatosis.

FAMILIAL PARTIAL LIPODYSTROPHY, DUNNIGAN TYPE Is also known as fpl2|lipoatrophic diabetes|lipodystrophy, reverse partial|fpld2|familial partial lipodystrophy type 2|lipodystrophy, familial, of limbs and lower trunk|dunnigan syndrome|lipodystrophy, familial partial, dunnigan type

Related symptoms:

  • Short stature
  • Micrognathia
  • Cataract
  • Hypertension
  • Hepatomegaly


SOURCES: OMIM ORPHANET MENDELIAN

More info about FAMILIAL PARTIAL LIPODYSTROPHY, DUNNIGAN TYPE

Low match OGDEN SYNDROME


Ogden syndrome is a rare, genetic progeroid syndrome characterized by a variable phenotype including postnatal growth delay, severe global developmental delay, hypotonia, non-specific dysmorphic facies with aged appearance and cryptorchidism, as well as cardiac arrthymias and skeletal anomalies. Patients typically present with widely opened fontanels, mainly truncal hypotonia, a waddling gait with hypertonia of the extremities, small hands and feet, broad great toes, scoliosis and redundant skin with lack of subcutaneous fat.

OGDEN SYNDROME Is also known as n-terminal acetyltransferase deficiency|premature aging appearance-developmental delay-cardiac arrhythmia syndrome|natd

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about OGDEN SYNDROME

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Other less relevant matches:

Low match ATYPICAL WERNER SYNDROME


Atypical Werner syndrome refers to a heterogeneous group of cases that are clinically diagnosed as Werner syndrome (WS; see this term) but do not carry WRN gene mutations. Similar to classical WS caused by WRN mutations, patients generally exhibit an aged appearance and common age-related disorders at earlier ages compared to the general population.

ATYPICAL WERNER SYNDROME Is also known as atypical progeroid syndrome

Related symptoms:

  • Short stature
  • Failure to thrive
  • Micrognathia
  • Hypertension
  • Skeletal muscle atrophy


SOURCES: ORPHANET MENDELIAN

More info about ATYPICAL WERNER SYNDROME

Low match FABRY DISEASE


Fabry disease (FD) is a progressive, inherited, multisystemic lysosomal storage disease characterized by specific neurological, cutaneous, renal, cardiovascular, cochleo-vestibular and cerebrovascular manifestations.

FABRY DISEASE Is also known as ceramide trihexosidase deficiency|hereditary dystopic lipidosis|fd|alpha-galactosidase a deficiency|diffuse angiokeratoma|gla deficiency|angiokeratoma corporis diffusum|anderson-fabry disease

Related symptoms:

  • Seizures
  • Short stature
  • Hearing impairment
  • Sensorineural hearing impairment
  • Pain


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about FABRY DISEASE

Low match HUTCHINSON-GILFORD PROGERIA SYNDROME


Hutchinson-Gilford progeria syndrome is a rare, fatal, autosomal dominant and premature aging disease, beginning in childhood and characterized by growth reduction, failure to thrive, a typical facial appearance (prominent forehead, protuberant eyes, thin nose with a beaked tip, thin lips, micrognathia and protruding ears) and distinct dermatologic features (generalized alopecia, aged-looking skin, sclerotic and dimpled skin over the abdomen and extremities, prominent cutaneous vasculature, dyspigmentation, nail hypoplasia and loss of subcutaneous fat).

HUTCHINSON-GILFORD PROGERIA SYNDROME Is also known as progeria|hgps

Related symptoms:

  • Intellectual disability
  • Short stature
  • Hearing impairment
  • Scoliosis
  • Growth delay


SOURCES: OMIM ORPHANET MENDELIAN

More info about HUTCHINSON-GILFORD PROGERIA SYNDROME

Low match SUPRAVALVULAR AORTIC STENOSIS


SupraValvar Aortic Stenosis (SVAS) is characterized by the narrowing of the aorta lumen (close to its origin) or other arteries (branch pulmonary arteries, coronary arteries). This narrowing of the aorta or pulmonary branches may impede blood flow, resulting in heart murmur and ventricular hypertrophy (in case of aorta involvement). The narrowing results from a thickening of the artery wall, which is not related to atherosclerosis.

SUPRAVALVULAR AORTIC STENOSIS Is also known as supravalvar aortic stenosis, eisenberg type|svas

Related symptoms:

  • Intellectual disability
  • Abnormal facial shape
  • Edema
  • Arrhythmia
  • Pulmonic stenosis


SOURCES: ORPHANET OMIM MENDELIAN

More info about SUPRAVALVULAR AORTIC STENOSIS

Low match HURLER SYNDROME


Hurler syndrome is the most severe form of mucopolysaccharidosis type 1 (MPS1; see this term), a rare lysosomal storage disease, characterized by skeletal abnormalities, cognitive impairment, heart disease, respiratory problems, enlarged liver and spleen, characteristic facies and reduced life expectancy.

HURLER SYNDROME Is also known as mpsih|mps1h|mps1-h|mucopolysaccharidosis type 1h|mucopolysaccharidosis type ih|hurler disease

Related symptoms:

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


SOURCES: OMIM ORPHANET MENDELIAN

More info about HURLER SYNDROME

Low match GRANGE SYNDROME


Grange syndrome is characterised by stenosis or occlusion of multiple arteries (including the renal, cerebral and abdominal vessels), hypertension, brachysyndactyly, syndactyly, increased bone fragility, and learning difficulties or borderline intellectual deficit. Congenital heart defects were also reported in some cases.

GRANGE SYNDROME Is also known as arterial occlusive disease, progressive, with hypertension, heart defects, bone fragility, and brachysyndactyly|grange occlusive arterial syndrome|progressive arterial occlusive disease-hypertension-heart defects-bone fragility-brachysyndactyly syndrome

Related symptoms:

  • Intellectual disability
  • Hypertelorism
  • Failure to thrive
  • Abnormal facial shape
  • Pain


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about GRANGE SYNDROME

Low match MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME


Megalencephaly-capillary malformation-polymicrogyria syndrome (MCAP) is a polymalfomative syndrome characterized by cutaneous capillary malformations, megalencephaly, cortical brain malformations (most distinctively polymicrogyria), abnormalities of somatic growth with body and brain asymmetry, developmental delay, and characteristic facial dysmorphism.

MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME Is also known as megalencephaly-cutis marmorata telangiectatica congenita syndrome|macrocephaly-capillary malformation syndrome|mcmtc|mcap|megalencephaly-capillary malformation syndrome|macrocephaly-cutis marmorata telangiectatica congenita syndrome|mcm

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Neoplasm
  • Failure to thrive
  • Muscular hypotonia


SOURCES: ORPHANET MENDELIAN

More info about MEGALENCEPHALY-CAPILLARY MALFORMATION-POLYMICROGYRIA SYNDROME

Top 5 symptoms//phenotypes associated to Abnormal facial shape and Coronary artery atherosclerosis

Symptoms // Phenotype % cases
Short stature Common - Between 50% and 80% cases
Hypertension Common - Between 50% and 80% cases
Congestive heart failure Common - Between 50% and 80% cases
Intellectual disability Common - Between 50% and 80% cases
Failure to thrive Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Abnormal facial shape and Coronary artery atherosclerosis. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Cardiomyopathy Arrhythmia Micrognathia Hepatic steatosis Myocardial infarction Osteolytic defects of the phalanges of the hand Hypertriglyceridemia Lipoatrophy Hypertrophic cardiomyopathy Decreased body weight Abnormality of the cardiovascular system Skeletal muscle atrophy Peripheral arterial stenosis Angina pectoris Thin skin Pain Dilatation Thin vermilion border Abnormality of the skeletal system Aortic regurgitation Edema Sensorineural hearing impairment Left ventricular hypertrophy Cataract Frontal bossing Global developmental delay Depressed nasal bridge Aortic valve stenosis Hyperinsulinemia Limitation of joint mobility Stroke Short clavicles Dyspnea Abdominal pain Hypertelorism Prominent superficial veins Growth delay Scoliosis Hyperlipidemia Hearing impairment Telangiectasia of the skin Diabetes mellitus Secondary amenorrhea Coarse facial features Generalized hirsutism Proptosis Prominent forehead Atherosclerosis Premature graying of hair Myalgia Acanthosis nigricans Aplasia/Hypoplasia of the skin Lipodystrophy Hepatomegaly Midface retrusion Splenomegaly Delayed puberty Behavioral abnormality Abnormality of the dentition Macrocephaly Heart murmur Insulin resistance

Rare Symptoms - Less than 30% cases


Premature ovarian insufficiency Ventricular tachycardia Reduced bone mineral density Sparse and thin eyebrow Abnormality of the thorax Glycosuria Long eyelashes Aplasia/Hypoplasia of the eyebrow Finger clinodactyly Pulmonary artery stenosis Supraventricular tachycardia Premature coronary artery atherosclerosis Hip dysplasia Increased bone mineral density Abnormality of the forehead Alopecia Osteoporosis Hypogonadism Mitral valve prolapse Hyperkeratosis Convex nasal ridge Hypotrichosis Retinal degeneration Short palm Thick eyebrow Fragile nails Carotid artery stenosis Abnormal EKG Transient ischemic attack Hydrocephalus Large earlobe Muscular hypotonia Arterial stenosis Pulmonic stenosis Abnormal mitral valve morphology Abnormal aortic valve morphology Coronary artery stenosis Wide mouth Multiple joint contractures Coxa valga Neoplasm Flexion contracture Kyphosis Cardiomegaly Osteopenia Conductive hearing impairment Joint stiffness Abnormal heart valve morphology Hemiplegia Carious teeth Carcinoma Cognitive impairment Optic atrophy Respiratory insufficiency Vomiting Diarrhea Renal insufficiency Headache Depressivity Constipation Corneal opacity Prominent supraorbital ridges Tachycardia Thick vermilion border Chest pain Mitral regurgitation Hypohidrosis Aminoaciduria Full cheeks Progressive hearing impairment Corneal dystrophy High, narrow palate Lack of skin elasticity Delayed eruption of teeth Minimal subcutaneous fat Macrotia Inguinal hernia Hernia Ventriculomegaly Ventricular septal defect Wide nasal bridge Decreased HDL cholesterol concentration Advanced eruption of teeth Narrow nasal ridge Loss of subcutaneous adipose tissue in limbs Dysmenorrhea Increased adipose tissue around the neck Increased intraabdominal fat Deeply set eye Absence of subcutaneous fat Generalized lipodystrophy Abnormality of lipid metabolism Insulin-resistant diabetes mellitus Increased facial adipose tissue Glomerulopathy High forehead Papule Hyperglycemia Narrow chest Infertility Spontaneous abortion Hirsutism Precocious atherosclerosis Supraventricular arrhythmia Round face Skeletal muscle hypertrophy Progeroid facial appearance Abnormality of the nail Ventricular arrhythmia Myopathy Polycystic ovaries Pectus carinatum Xanthomatosis Reduced subcutaneous adipose tissue Pancreatitis Severe global developmental delay Dental crowding Dolichocephaly Abnormal pyramidal sign Camptodactyly of finger Synophrys Retinopathy Abnormality of eye movement Craniosynostosis Nyctalopia Prolonged QT interval Pallor Broad-based gait Mental deterioration Apnea Elevated hepatic transaminase Arteriovenous malformation Hepatosplenomegaly Umbilical hernia Skeletal dysplasia Kyphoscoliosis Glaucoma Pes cavus Recurrent respiratory infections Pneumonia Genu valgum Abnormality of skin pigmentation Nevus flammeus Abnormality of the skin Recurrent otitis media Hypertrichosis Hypodontia Growth hormone deficiency Progressive neurologic deterioration Interphalangeal joint contracture of finger Nail dysplasia Intellectual disability, profound Cyanosis Lumbar hyperlordosis Abnormality of the ribs Microdontia Progressive visual loss Asthma Osteoarthritis Aplasia/Hypoplasia of the cerebellum Cutis marmorata Hypermelanotic macule Broad nasal tip Macroglossia Sleep disturbance Neurodegeneration Everted lower lip vermilion Foot polydactyly Inability to walk Wide nose Long philtrum Dry skin Visual loss Visceral angiomatosis Cerebral ischemia Generalized osteoporosis Thin nail Hip pain Aplastic clavicle Arteriosclerosis Carcinoid tumor Hypercholesterolemia Prolonged prothrombin time Relative macrocephaly Dermal atrophy Decreased serum estradiol Thin bony cortex Enlarged joints Aplasia/Hypoplasia of the earlobes Small face Nasal speech Sinus tachycardia Ovoid vertebral bodies Intracranial hemorrhage Hyperphosphatemia Down-sloping shoulders Absent eyelashes Metaphyseal widening Thrombocytosis Alopecia of scalp Renal cell carcinoma Hypoplastic nipples Keratoconjunctivitis sicca Thin ribs Scleroderma Exertional dyspnea Decreased testosterone in males Corneal arcus High pitched voice Abnormal form of the vertebral bodies Short neck Anteverted nares Delayed speech and language development Feeding difficulties Aspiration Hypergonadotropic hypogonadism Supravalvular aortic stenosis Hypogonadotrophic hypogonadism Peripheral pulmonary artery stenosis Hydrops fetalis Abnormality of nervous system morphology Tapering pointed ends of distal finger phalanges Arteriosclerosis of small cerebral arteries Regional abnormality of skin Abnormal trabecular bone morphology Intermittent claudication Insulin-resistant diabetes mellitus at puberty Absence of pubertal development Osteolysis Narrow nasal tip Bilateral coxa valga Craniofacial disproportion Old-aged sensorineural hearing impairment Reticulated skin pigmentation Hypoplastic facial bones Prominent scalp veins Bird-like facies Mitral valve calcification Parietal bossing Widely patent fontanelles and sutures Split hand Delayed tarsal ossification Encephalocele Abnormal mandible coronoid process morphology Delayed ossification of the hand bones Abnormal nerve conduction velocity Anterior open bite Abnormal mandibular ramus morphology Meckel diverticulum Abnormality of premolar morphology Stiff interphalangeal joints Sclerosis of skull base Abnormality of the tympanic membrane Narrow pelvis bone Abnormality of glycosaminoglycan metabolism Flared nostrils Increased size of nasopharyngeal adenoids Abnormality of the wing of the ilium Large sella turcica Difficulty standing Brachydactyly Prominent sternum Recurrent ear infections Broad femoral neck Delayed ossification of carpal bones Diaphyseal thickening Abnormal diaphysis morphology Specific learning disability Recurrent fractures Retinal fold Syndactyly Chronic rhinitis Abnormal heart morphology Patent ductus arteriosus Biconcave vertebral bodies Mucopolysacchariduria Clinodactyly Large face Anterior rib cupping J-shaped sella turcica Rhinorrhea Enlarged tonsils Abnormality of the pubic bone Hypoplasia of the femoral head Calcification of falx cerebri Enlarged vertebral pedicles Abnormality of the tonsils C1-C2 subluxation Deformed humerus Dermatan sulfate excretion in urine Hypoplastic cervical vertebrae Cervical subluxation Mandibular condyle hypoplasia Abnormality of lysosomal metabolism Flaring of rib cage Broad ischia Abnormality of joint mobility Abnormality of mucopolysaccharide metabolism Lumbar kyphosis Abnormality of the gingiva Cervical myelopathy Atlantoaxial dislocation Broad long bone diaphyses Hip subluxation Heparan sulfate excretion in urine Abnormal hand morphology Enlargement of the wrists Abnormality of the middle ear ossicles Calvarial hyperostosis Abnormal CNS myelination Thoracolumbar kyphoscoliosis Hernia of the abdominal wall Bullet-shaped phalanges of the hand Urinary glycosaminoglycan excretion Proximal tapering of metacarpals Short mandibular rami Cervical kyphosis Cutaneous syndactyly Abnormality of peripheral nerve conduction Hand polydactyly Thickened calvaria Language impairment Stridor Toe walking Metatarsus adductus Flared metaphysis Restrictive ventilatory defect Arthropathy Polymicrogyria Joint hyperflexibility Spinal canal stenosis Rhinitis Thoracic scoliosis Protruding tongue Hypoplasia of the odontoid process Facial asymmetry Back pain Recurrent upper respiratory tract infections Finger syndactyly Spastic paraparesis Chronic diarrhea Thickened skin Abnormality of epiphysis morphology Gingival overgrowth Exotropia Thick skull base Elbow flexion contracture Arnold-Chiari malformation Increased intracranial pressure Abnormality of dental enamel Opacification of the corneal stroma Coxa vara Cerebral palsy Widely spaced teeth Sleep apnea Hyperammonemia Toe syndactyly Abnormality of cardiovascular system morphology Myelopathy Flared iliac wings Beaking of vertebral bodies Communicating hydrocephalus Upper airway obstruction Hypoplastic ilia Conical tooth Cor pulmonale Foam cells Abnormality of the respiratory system Pulmonary edema Seborrheic dermatitis Endocardial fibroelastosis Bicuspid aortic valve Constrictive median neuropathy Hypoplasia of teeth Sagittal craniosynostosis Tracheal stenosis Dysostosis multiplex Renovascular hypertension Perimembranous ventricular septal defect Renal artery stenosis Palpebral edema Intellectual disability, borderline Protuberant abdomen Peripheral visual field loss Shallow orbits Gastritis Cutaneous finger syndactyly Diastasis recti Increased susceptibility to fractures Abnormality of the elbow Recurrent lower respiratory tract infections Obstructive sleep apnea Abnormality of the skull Abnormality of the clavicle Gingivitis Abnormal vertebral morphology Achalasia Hypermetropia Ovarian neoplasm Laryngomalacia Abnormality of the voice Rocker bottom foot Calf muscle hypertrophy Decreased fertility Sparse body hair Prematurely aged appearance Narrow face Neoplasm of the lung Meningioma Renal neoplasm Osteosarcoma Abnormality of the cerebral vasculature Pili torti Neoplasm of the skin Abnormality of the hair Chondrocalcinosis Cardiogenic shock Torsade de pointes Unilateral cryptorchidism Acetabular dysplasia Everted upper lip vermilion Capillary malformation Abnormality of the nares Abnormal head movements Skin ulcer Enlarged naris Facial wrinkling Pes planus Congenital cataract Type II diabetes mellitus Abnormality of retinal pigmentation Abnormality of the testis Exercise-induced myalgia Shuffling gait Mandibular prognathia Peripheral neuropathy Fever Fatigue Posteriorly rotated ears Hyperhidrosis Hypothyroidism Arthralgia Seizures Arthritis Anxiety Proteinuria Abnormality of the nervous system Abnormality of the kidney Developmental regression Anemia Abnormality of circulating leptin level White forelock Abnormality of the Achilles tendon Abnormality of the pulmonary artery Abnormal hair quantity Neoplasm of the breast Aortic valve calcification Fasting hyperinsulinemia Abnormal hair whorl Neoplasm of the small intestine Sclerosis of hand bone Subcutaneous calcification Neoplasm of the thyroid gland Intervertebral disc degeneration Premature arteriosclerosis Neoplasm of the oral cavity Progressive clavicular acroosteolysis Patchy hypo- and hyperpigmentation Thick upper lip vermilion Excessive daytime somnolence Cough Enlarged peripheral nerve Abnormality of skeletal muscle fiber size Osteopoikilosis Adipose tissue loss Abnormality of complement system Sunken cheeks Loss of truncal subcutaneous adipose tissue Myelin tomacula Congenital generalized lipodystrophy Labial pseudohypertrophy Increased intramuscular fat Generalized hypotonia Microcephaly Cryptorchidism Low-set ears Eclampsia Abnormality of the menstrual cycle Epicanthus Proximal upper limb muscle hypertrophy Abnormal atrioventricular conduction Decreased serum leptin Accelerated atherosclerosis Acroosteolysis of distal phalanges (feet) Decreased adiponectin level Muscle hypertrophy of the lower extremities Obesity Acute pancreatitis Pectus excavatum Epidermal acanthosis Cranial nerve paralysis Cellulitis Hyperuricemia Maternal diabetes Hyperlipoproteinemia High palate Downslanted palpebral fissures Ventricular extrasystoles Delayed gross motor development Low anterior hairline Microretrognathia Torticollis Cutis laxa Shock Scrotal hypoplasia Coarse hair Fine hair Deep philtrum Redundant skin Broad hallux Delayed cranial suture closure Poor eye contact Short columella Stereotypy Narrow forehead Atrial septal defect Neonatal hypotonia Hypertonia Cerebral atrophy Recurrent infections Encephalopathy Delayed skeletal maturation Thin upper lip vermilion Muscular hypotonia of the trunk Waddling gait Postnatal growth retardation Autistic behavior Lethargy Abnormality of the foot Small hand Highly arched eyebrow Underdeveloped nasal alae Skin rash Prominent nasal bridge Dilated cardiomyopathy Retinal vascular tortuosity Primary hypothyroidism Biventricular hypertrophy Abnormal endocardium morphology Abnormality of cardiovascular system physiology Decreased female libido Vascular skin abnormality Corneal crystals Conjunctival telangiectasia Limb pain Abnormality of temperature regulation Nephrogenic diabetes insipidus Decreased glomerular filtration rate Vascular tortuosity Distal renal tubular acidosis Microalbuminuria Dysesthesia Reduced sperm motility Gastrointestinal dysmotility Abnormality of the nose Restrictive cardiomyopathy Abnormal myocardium morphology High-frequency hearing impairment Asymmetric septal hypertrophy Periorbital fullness T-wave inversion Abnormal cornea morphology Miosis Abnormal renal physiology Chronic pain Tubulointerstitial fibrosis Abnormal thrombosis Abnormality of the renal tubule Increased blood urea nitrogen Angiokeratoma Chronic fatigue Cornea verticillata Abnormal common carotid artery morphology Abnormal ST segment Increased carotid artery intimal medial thickness Increased glomerular filtration rate Abnormality of the common coagulation pathway Abnormal glomerular filtration rate Short nose Heavy proteinuria Malar flattening Dementia Narrow mouth Sparse hair Microtia Hip dislocation Acroparesthesia Tenesmus Obstructive lung disease Concentric hypertrophic cardiomyopathy Impaired temperature sensation Hyposthenuria Shortened QT interval Angiokeratoma corporis diffusum Decreased lacrimation Shortened PR interval Mucosal telangiectasiae Left ventricular septal hypertrophy Unexplained fevers ST segment depression Functional abnormality of the gastrointestinal tract Impaired renal concentrating ability Abnormality of glycosphingolipid metabolism Hyperkeratotic papule Tortuosity of conjunctival vessels Abnormality of femur morphology Myocardial fibrosis Pruritus Bradycardia Atrial fibrillation Palpitations Abnormal lung morphology Subcutaneous nodule Anorexia Lymphedema Fasciculations Ventricular hypertrophy Abnormal autonomic nervous system physiology Exercise intolerance Purpura Abnormal intestine morphology Ischemic stroke Tinnitus Thick lower lip vermilion Nephrotic syndrome Atrioventricular block Nausea Abnormality of the cerebral white matter Malabsorption Nausea and vomiting Paresthesia Vertigo Stage 5 chronic kidney disease Bulbous nose Hypotension Hematuria Nephropathy Muscle cramps Abdominal distention Sudden cardiac death Syncope Urinary incontinence Easy fatigability Chronic kidney disease Sinus bradycardia Elevated serum creatinine Wheezing Aortic root aneurysm Xerostomia Renal tubular dysfunction Edema of the lower limbs Tubulointerstitial nephritis Tubular atrophy Celiac disease Abnormality of the gastrointestinal tract Oligospermia Heat intolerance Reduced ejection fraction Clubbing of fingers Chronic obstructive pulmonary disease Renal tubular acidosis Orthostatic hypotension Abnormality of the hand Diabetes insipidus Glomerulosclerosis Polydipsia Personality changes Clubbing Impaired vibratory sensation Tricuspid regurgitation Polyuria Progressive sensorineural hearing impairment Anhidrosis Emphysema Loss of consciousness Bundle branch block Impotence Elevated erythrocyte sedimentation rate Interstitial pulmonary abnormality Asymmetric growth



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