Carcinoma, and Sparse and thin eyebrow

Diseases related with Carcinoma and Sparse and thin eyebrow

In the following list you will find some of the most common rare diseases related to Carcinoma and Sparse and thin eyebrow that can help you solving undiagnosed cases.


Top matches:

High match KID SYNDROME


Keratitis (and hystrix-like) ichthyosis deafness (KID/HID) syndrome is a rare congenital ectodermal disorder characterized by vascularizing keratitis, hyperkeratotic skin lesions and hearing loss.

KID SYNDROME Is also known as ichthyosis hystrix rheydt type|keratitis-ichthyosis-deafness/hystrix-like ichthyosis-deafness syndrome|senter syndrome|kid/hid syndrome|kid syndrome, autosomal dominant

Related symptoms:

  • Intellectual disability
  • Short stature
  • Hearing impairment
  • Neoplasm
  • Sensorineural hearing impairment


SOURCES: OMIM ORPHANET MENDELIAN

More info about KID SYNDROME

High match CARTILAGE-HAIR HYPOPLASIA


Cartilage-hair hypoplasia is a disease affecting the bone metaphyses causing small stature from birth.

CARTILAGE-HAIR HYPOPLASIA Is also known as autosomal recessive metaphyseal chondrodysplasia|metaphyseal chondrodysplasia, mckusick type

Related symptoms:

  • Intellectual disability
  • Short stature
  • Scoliosis
  • Growth delay
  • Neoplasm


SOURCES: OMIM ORPHANET MENDELIAN

More info about CARTILAGE-HAIR HYPOPLASIA

High 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

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Other less relevant matches:

High match SCHÖPF-SCHULZ-PASSARGE SYNDROME


Schöpf-Schulz-Passarge syndrome (SSPS) is a rare autosomal recessive ectodermal dysplasia characterized by multiple eyelid apocrine hidrocystomas, palmoplantar keratoderma, hypotrichosis, hypodontia and nail dystrophy.

SCHÖPF-SCHULZ-PASSARGE SYNDROME Is also known as palmoplantar keratoderma-cystic eyelids-hypodontia-hypotrichosis syndrome|keratosis palmoplantaris with cystic eyelids, hypodontia, and hypotrichosis|eccrine tumors with ectodermal dysplasia|ssps|palmoplantar hyperkeratosis-cystic eyelids-hypodontia-hypot

Related symptoms:

  • Neoplasm
  • Alopecia
  • Hyperhidrosis
  • Hyperkeratosis
  • Carcinoma


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about SCHÖPF-SCHULZ-PASSARGE SYNDROME

Medium match MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB; MEN2B


Multiple endocrine neoplasia type IIB (MEN2B) is an autosomal dominant hamartoneoplastic syndrome characterized by aggressive medullary thyroid carcinoma (MTC), pheochromocytoma, mucosal neuromas, and thickened corneal nerves. Most affected individuals have characteristic physical features, including full lips, thickened eyelids, high-arched palate, and marfanoid habitus. Other more variable features include skeletal anomalies and gastrointestinal problems (review by Morrison and Nevin, 1996).For a discussion of genetic heterogeneity of multiple endocrine neoplasia (MEN), see MEN1 (OMIM ).

MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB; MEN2B Is also known as men iib|multiple endocrine neoplasia, type iii, formerly|wagenmann-froboese syndrome|men3, formerly|neuromata, mucosal, with endocrine tumors

Related symptoms:

  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Scoliosis
  • Neoplasm


SOURCES: OMIM MENDELIAN

More info about MULTIPLE ENDOCRINE NEOPLASIA, TYPE IIB; MEN2B

Medium 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 PACHYONYCHIA CONGENITA 2; PC2


Pachyonychia congenita (PC) is an autosomal dominant genodermatosis with the main clinical features of hypertrophic nail dystrophy, painful and highly debilitating plantar keratoderma, oral leukokeratosis, and a variety of epidermal cysts. Although the condition had previously been subdivided clinically into Jadassohn-Lewandowsky PC type 1 and Jackson-Lawler PC type 2, patients with PC were later found to have a mixed constellation of both types, leading to a classification of PC based on genotype (summary by Sybert, 2010; Eliason et al., 2012; McLean et al., 2011).For a discussion of genetic heterogeneity of pachyonychia congenita, see {167200}. Historical Classification of Pachyonychia CongenitaGorlin et al. (1976) suggested that 2 distinct syndromes are subsumed under the designation pachyonychia congenita. PC type 1, the Jadassohn-Lewandowsky type, shows oral leukokeratosis. PC type 2, the Jackson-Lawler type, has natal teeth and epidermoid cysts (cylindromas), but no oral leukoplakia. Corneal dystrophy may be a feature exclusively of the Jackson-Lawler type.Smith et al. (1998) stated that PC type 2, in contrast to PC type 1, has minimal oral involvement and milder keratoderma, and multiple steatocystomas (OMIM ) is a major clinical feature. Steatocystoma, also known as eruptive vellus cyst, is a cystic hamartoma lined by sebaceous ductal epithelium.On the basis of a study of 13 patients with PC type 1 or type 2, Terrinoni et al. (2001) concluded that the presence of pilosebaceous cysts following puberty is the best indicator of PC type 2; prepubescent patients are more difficult to classify due to the lack of cysts. Natal teeth are indicative of PC type 2, although their absence does not preclude the PC type 2 diagnosis.

PACHYONYCHIA CONGENITA 2; PC2 Is also known as pachyonychia congenita, jackson-lawler type, formerly

Related symptoms:

  • Hyperhidrosis
  • Hyperkeratosis
  • Nail dystrophy
  • Nail dysplasia
  • Sparse scalp hair


SOURCES: OMIM MENDELIAN

More info about PACHYONYCHIA CONGENITA 2; PC2

Low match FAMILIAL CUTANEOUS TELANGIECTASIA AND OROPHARYNGEAL CANCER PREDISPOSITION SYNDROME


Familial cutaneous telangiectasia and oropharyngeal cancer predisposition syndrome is a rare, inherited cancer-predisposing syndrome characterized by an early development of cutaneous telangiectasia, mild dental and nail anomalies, patchy alopecia over the affected skin areas and increased lifetime risk for oropharyngeal cancer. Other types of cancer have also been reported.

FAMILIAL CUTANEOUS TELANGIECTASIA AND OROPHARYNGEAL CANCER PREDISPOSITION SYNDROME Is also known as telangiectasia, cutaneous, and cancer syndrome, familial

Related symptoms:

  • Neoplasm
  • Alopecia
  • Carcinoma
  • Carious teeth
  • Convex nasal ridge


SOURCES: ORPHANET OMIM MENDELIAN

More info about FAMILIAL CUTANEOUS TELANGIECTASIA AND OROPHARYNGEAL CANCER PREDISPOSITION SYNDROME

Low match OCULOCUTANEOUS ALBINISM TYPE 6


Oculocutaneous albinism type 6 (OCA6) is a type of oculocutaneous albinism, recently discovered in one Chinese family, characterized by light hair at birth that darkens with age, white skin, transparent irides, photophobia, nystagmus, foveal hypoplasia and reduced visual acuity and that is due to mutations in the SLC24A5 gene (15q21.1).

OCULOCUTANEOUS ALBINISM TYPE 6 Is also known as oca6

Related symptoms:

  • Nystagmus
  • Strabismus
  • Visual impairment
  • Reduced visual acuity
  • Photophobia


SOURCES: ORPHANET OMIM MENDELIAN

More info about OCULOCUTANEOUS ALBINISM TYPE 6

Low match BIRT-HOGG-DUBÉ SYNDROME


Birt-Hogg-Dube (BHD) syndrome is characterized by skin lesions, kidney tumors, and pulmonary cysts that may be associated with pneumothorax. It is a rare clinicopathologic condition named after the three Canadian physicians who reported the syndrome in 1977.

BIRT-HOGG-DUBÉ SYNDROME Is also known as hornstein-knickenberg syndrome|fibrofolliculomas with trichodiscomas and acrochordons

Related symptoms:

  • Neoplasm
  • Pain
  • Carcinoma
  • Papule
  • Renal cyst


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about BIRT-HOGG-DUBÉ SYNDROME

Top 5 symptoms//phenotypes associated to Carcinoma and Sparse and thin eyebrow

Symptoms // Phenotype % cases
Neoplasm Common - Between 50% and 80% cases
Alopecia Uncommon - Between 30% and 50% cases
Pain Uncommon - Between 30% and 50% cases
Neoplasm of the skin Uncommon - Between 30% and 50% cases
Hyperhidrosis Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Carcinoma and Sparse and thin eyebrow. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Hyperkeratosis Basal cell carcinoma Short stature Squamous cell carcinoma Nail dysplasia Aganglionic megacolon Hypohidrosis Renal cell carcinoma Intellectual disability Convex nasal ridge Hypotrichosis Constipation Diarrhea Scoliosis Cardiomyopathy Abnormality of the skeletal system Thin nail Hypertension Carious teeth Visual impairment Photophobia Sparse hair Nail dystrophy Hearing impairment Sensorineural hearing impairment

Rare Symptoms - Less than 30% cases


Coarse facial features Emphysema Cataract Abnormal facial shape Thick vermilion border Thrombocytosis Seizures Metaphyseal widening Abnormality of retinal pigmentation Cafe-au-lait spot Narrow chest Hypopigmentation of the skin Malabsorption Subcutaneous nodule Congestive heart failure Joint laxity Macrotia Prominent forehead Thick lower lip vermilion Dilatation Respiratory insufficiency Hyperlordosis Proptosis Kyphosis Abnormal lung morphology Bird-like facies Angina pectoris Medullary thyroid carcinoma Papule Transient ischemic attack Abnormal EKG Palmoplantar hyperkeratosis Onycholysis Heart murmur Hyperlipidemia Aminoaciduria Anemia Midface retrusion Ridged nail Myocardial infarction Abnormality of the cardiovascular system Corneal dystrophy Chest pain Hypodontia Delayed puberty Stroke Hypertrophic cardiomyopathy Achalasia Dyspnea Left ventricular hypertrophy Thick eyebrow Cognitive impairment Pes cavus Keratoconjunctivitis sicca Alopecia of scalp Reduced tendon reflexes Osteolysis Sparse eyelashes Thickened skin Fine hair Oral leukoplakia Palmoplantar keratoderma Abnormality of the hair Nevus Arthritis Delayed eruption of teeth Aplasia/Hypoplasia of the eyebrow Delayed skeletal maturation Failure to thrive Abnormality of the dentition Growth delay Visual loss Strabismus Muscular hypotonia Syncope Glomerulosclerosis Cylindroma Mitral regurgitation Renal neoplasm Palpitations Parathyroid adenoma Atrial fibrillation Ventricular hypertrophy Nephrotic syndrome Mitral valve prolapse Hypotension Urinary incontinence Sudden cardiac death Lymphedema Abdominal distention Polydipsia Muscle cramps Intestinal polyposis Nephropathy Hematuria Bulbous nose Tachycardia Nausea Stage 5 chronic kidney disease Vertigo Paresthesia Anorexia Bradycardia Abnormality of the hand Reduced bone mineral density Actinic keratosis Fibrofolliculoma Prominent supraorbital ridges Chronic kidney disease Atrioventricular block Renal cyst Easy fatigability Tinnitus Ventricular arrhythmia Colon cancer Multiple lipomas Hemiplegia Ischemic stroke Fasciculations Abnormality of abdomen morphology Skin tags Progressive hearing impairment Polyneuropathy Abnormal foveal morphology on macular OCT Abnormal intestine morphology Aortic regurgitation Ventricular tachycardia Purpura Exercise intolerance Nausea and vomiting Spontaneous abortion Abnormal autonomic nervous system physiology Abnormality of the skin Failure to thrive in infancy Pneumothorax Ganglioneuroma Papillary renal cell carcinoma Ganglioneuromatosis Prominent corneal nerve fibers Inguinal freckling Elevated urinary epinephrine Subcutaneous neurofibromas Neuroma Proximal femoral epiphysiolysis Abnormality of the parathyroid gland Nodular goiter Elevated calcitonin Schizencephaly Colonic diverticula Peripheral neuropathy Clear cell renal cell carcinoma Lisch nodules Parathyroid hyperplasia Pheochromocytoma Pulmonary sequestration Thyroid carcinoma Goiter Spontaneous pneumothorax Neoplasm of the endocrine system Flushing Freckling Neurofibromas Disproportionate tall stature Multiple mucosal neuromas Fever Abnormality of the cerebral white matter Myalgia Acne Hemiparesis Fibroma Corneal opacity Prominent nasal bridge Cough Skin rash Developmental regression Abnormal iris pigmentation Abnormality of the kidney Abnormality of the nervous system Proteinuria Anxiety Arthralgia Optic atrophy Mandibular prognathia Hypothyroidism Abdominal pain Posteriorly rotated ears Arrhythmia Depressivity Headache Renal insufficiency Behavioral abnormality Vomiting Edema Intestinal polyp Fatigue Pruritus Diabetes insipidus Personality changes Reduced sperm motility ST segment depression Unexplained fevers Mucosal telangiectasiae Concentric hypertrophic cardiomyopathy Melanoma Coronary artery stenosis Shortened PR interval Decreased lacrimation Angiokeratoma corporis diffusum Shortened QT interval Hyposthenuria Impaired temperature sensation Obstructive lung disease Angiokeratoma Melanocytic nevus Impaired renal concentrating ability Increased blood urea nitrogen Distal renal tubular acidosis Vascular tortuosity Decreased glomerular filtration rate Nephrogenic diabetes insipidus Abnormality of temperature regulation Limb pain Corneal crystals Retinal vascular tortuosity Vascular skin abnormality Decreased female libido Abnormality of cardiovascular system physiology Abnormal endocardium morphology Biventricular hypertrophy Functional abnormality of the gastrointestinal tract Abnormality of glycosphingolipid metabolism Microalbuminuria Abnormality of the common coagulation pathway Palmoplantar hyperhidrosis Epidermoid cyst Folliculitis Dry hair Subungual hyperkeratosis Hamartoma Hypoplasia of dental enamel Natal tooth Hoarse voice Telangiectasia Sparse scalp hair Cornea verticillata Breast carcinoma Abnormal glomerular filtration rate Patchy alopecia Abnormality of the forehead Heavy proteinuria Hyperkeratotic papule Tortuosity of conjunctival vessels Abnormal bleeding Reduced visual acuity Left ventricular septal hypertrophy Tenesmus Acroparesthesia Increased glomerular filtration rate Nystagmus Abnormal common carotid artery morphology Sebaceous gland carcinoma Abnormal ST segment Increased carotid artery intimal medial thickness Onychomycosis Primary hypothyroidism Albinism Clubbing Progressive sensorineural hearing impairment Tubulointerstitial nephritis Edema of the lower limbs Renal tubular dysfunction Xerostomia Abnormality of lipid metabolism Aortic root aneurysm Wheezing Renal tubular acidosis Glycosuria Abnormal heart valve morphology Glomerulopathy Telangiectasia of the skin Celiac disease Orthostatic hypotension Interstitial pulmonary abnormality Tubular atrophy Elevated erythrocyte sedimentation rate Coronary artery atherosclerosis Impotence Bundle branch block Generalized hypopigmentation Papilloma Loss of consciousness Anhidrosis Abnormal fundus morphology Polyuria Steatocystoma multiplex Aplasia/Hypoplasia of the macula Tricuspid regurgitation Impaired vibratory sensation Elevated serum creatinine Abnormality of the gastrointestinal tract Conjunctival telangiectasia Abnormal mitral valve morphology Supraventricular arrhythmia Dysesthesia Abnormal cornea morphology Abnormality of the renal tubule Abnormal thrombosis Tubulointerstitial fibrosis Chronic pain Abnormal renal physiology Miosis T-wave inversion Severe vision loss Abnormal aortic valve morphology Gastrointestinal dysmotility Periorbital fullness Asymmetric septal hypertrophy Oligospermia Chronic obstructive pulmonary disease Large earlobe Supraventricular tachycardia Heat intolerance Reduced ejection fraction Peripheral arterial stenosis Clubbing of fingers Sinus bradycardia High-frequency hearing impairment Hypoplasia of the fovea Chronic fatigue Abnormality of femur morphology Abnormality of the nose Restrictive cardiomyopathy Abnormal myocardium morphology Myocardial fibrosis Sinus tachycardia High, narrow palate Hypocalcemia Abnormality of the hip bone Tibial bowing Limited elbow extension Femoral bowing Mesomelia Short thorax Cone-shaped epiphysis Portal hypertension Genu varum Abnormality of pelvic girdle bone morphology Disproportionate short-limb short stature Sacral dimple Abnormal palate morphology Accelerated skeletal maturation Short ribs Metaphyseal dysplasia Lymphopenia Gingival overgrowth Rhizomelia Abnormality of epiphysis morphology Bronchiectasis Bowing of the long bones Abnormal form of the vertebral bodies Abnormality of the metaphysis Depressed nasal ridge Blue sclerae Lumbar hyperlordosis Abnormality of the ribs Decreased antibody level in blood Gastrointestinal hemorrhage High hypermetropia Macrocytic anemia Postural instability Aplasia/Hypoplasia affecting the eye Neonatal short-limb short stature Congenital hypoplastic anemia Spinal dysraphism Large face Hypersplenism Normocytic anemia Mucopolysacchariduria Abnormal diaphysis morphology Diaphyseal thickening Bronchiolitis Abnormality of chromosome stability Metaphyseal cupping Cellular immunodeficiency Metaphyseal chondrodysplasia Aplasia/Hypoplasia of the abdominal wall musculature Hodgkin lymphoma Abnormality of the pancreas Aplastic anemia B-cell lymphoma Generalized joint laxity Tracheal stenosis Fair hair Heart block Upper limb undergrowth Overweight Exocrine pancreatic insufficiency Distal arthrogryposis Esophageal atresia Hypoplasia of the odontoid process Anal stenosis Lymphoma Neutropenia Abnormally ossified vertebrae Keratitis Recurrent corneal erosions Corneal neovascularization Dystrophic fingernails Hypoplastic fingernail Furrowed tongue Dystrophic toenail Corneal erosion Abnormal eyelash morphology Severe hearing impairment Cellulitis Macule Hemiplegia/hemiparesis Hypoplastic toenails Absent eyebrow Congenital sensorineural hearing impairment Squamous cell carcinoma of the skin Scaling skin Urticaria Conjunctivitis Knee flexion contracture Elbow flexion contracture Skin ulcer Progressive visual loss Ichthyosis Severe global developmental delay Scarring Erythema Cerebellar hypoplasia Blindness Cryptorchidism Abnormality of the tongue Keratoconjunctivitis Small hand Thrombocytopenia Short palm Joint hypermobility Micromelia Joint hyperflexibility Arthrogryposis multiplex congenita Leukemia Pectus carinatum Abnormal cardiac septum morphology Low-set, posteriorly rotated ears EEG abnormality Skeletal dysplasia Brachycephaly Severe short stature Pneumonia Recurrent infections Corneal scarring Depressed nasal bridge Recurrent bacterial skin infections Generalized hyperkeratosis Corneal ulceration Moderate hearing impairment Trichiasis Abnormality of corneal stroma Epicanthus Immunodeficiency Hepatomegaly Wide nasal bridge Myopia Anteverted nares Short neck Splenomegaly Abnormal bone ossification Hypoplastic anemia Pectus excavatum Enlarged joints Widely patent fontanelles and sutures Intermittent claudication Corneal arcus Decreased testosterone in males Premature coronary artery atherosclerosis Absence of subcutaneous fat Hip pain Aplastic clavicle Narrow nasal ridge Arteriosclerosis Carcinoid tumor Prolonged prothrombin time Decreased serum estradiol Thin bony cortex Precocious atherosclerosis Mitral valve calcification Aplasia/Hypoplasia of the earlobes Small face Generalized osteoporosis Lack of skin elasticity Prominent superficial veins Osteolytic defects of the phalanges of the hand Ovoid vertebral bodies Hyperphosphatemia Down-sloping shoulders Fragile nails Absent eyelashes Short clavicles Hypoplastic nipples Thin ribs Parietal bossing Prominent scalp veins Lipoatrophy Ovarian neoplasm Myopathy High palate Ptosis Generalized hypotonia Global developmental delay Poroma Apocrine hidrocystoma Narrow nail Abnormality of primary teeth Trichodysplasia Facial telangiectasia Plantar hyperkeratosis Toenail dysplasia Premature loss of primary teeth Small nail Hypoplastic facial bones Ectodermal dysplasia Abnormality of the eye Tapering pointed ends of distal finger phalanges Arteriosclerosis of small cerebral arteries Regional abnormality of skin Abnormal trabecular bone morphology Insulin-resistant diabetes mellitus at puberty Absence of pubertal development Carotid artery stenosis Narrow nasal tip Bilateral coxa valga Craniofacial disproportion Old-aged sensorineural hearing impairment Reticulated skin pigmentation Scleroderma Exertional dyspnea Abnormal T cell morphology Flexion contracture Dilated cardiomyopathy Hip dislocation Microtia Joint stiffness Conductive hearing impairment Osteopenia Narrow mouth Hypogonadism Osteoporosis Dementia Malar flattening Short nose Macrocephaly Skeletal muscle atrophy Micrognathia Infertility Pulmonary lymphoma Susceptibility to chickenpox Flaring of lower rib cage Absent pubertal growth spurt Abnormality of humoral immunity Biconvex vertebral bodies Severe T-cell immunodeficiency Sparse facial hair Impaired lymphocyte transformation with phytohemagglutinin Metaphyseal dysostosis Non-Hodgkin lymphoma Long fibula Narrow vertebral interpedicular distance Abnormality of the distal phalanx of finger Hypermetropia Thin vermilion border Prolonged QT interval Coxa valga Premature graying of hair High pitched voice Multiple joint contractures Abnormality of the thorax Premature ovarian insufficiency Hyperinsulinemia Lipodystrophy Intracranial hemorrhage Nasal speech Dermal atrophy Relative macrocephaly Hypercholesterolemia Acanthosis nigricans Atherosclerosis Hypogonadotrophic hypogonadism Hepatic steatosis Thin skin Limitation of joint mobility Growth hormone deficiency Cyanosis Cardiomegaly Hypertriglyceridemia Osteoarthritis Broad-based gait Hypergonadotropic hypogonadism Decreased body weight Dental crowding Insulin resistance Aortic valve stenosis Aspiration Increased bone mineral density Salivary gland oncocytoma



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Intellectual disability, severe and Intellectual disability, moderate, related diseases and genetic alterations Macrocephaly and High myopia, related diseases and genetic alterations Cardiomyopathy and Hypopigmentation of the skin, related diseases and genetic alterations Spasticity and Interphalangeal joint contracture of finger, related diseases and genetic alterations Nystagmus and Spina bifida, related diseases and genetic alterations Cataract and Congestive heart failure, related diseases and genetic alterations Abnormal facial shape and Bradykinesia, related diseases and genetic alterations

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