Breast carcinoma, and Anxiety

Diseases related with Breast carcinoma and Anxiety

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


Top matches:

High match LYNCH SYNDROME


LYNCH SYNDROME Is also known as coca2|colon cancer, familial nonpolyposis, type 2|fcc2

Related symptoms:

  • Seizures
  • Neoplasm
  • Muscular hypotonia
  • Flexion contracture
  • Visual impairment


SOURCES: ORPHANET OMIM MENDELIAN

More info about LYNCH SYNDROME

High match ATAXIA-TELANGIECTASIA


Ataxia-telangiectasia is the association of severe combined immunodeficiency (affecting mainly the humoral immune response) with progressive cerebellar ataxia. It is characterised by neurological signs, telangiectasias, increased susceptibility to infections and a higher risk of cancer.

ATAXIA-TELANGIECTASIA Is also known as at1|louis-bar syndrome

Related symptoms:

  • Intellectual disability
  • Seizures
  • Short stature
  • Microcephaly
  • Scoliosis


SOURCES: ORPHANET OMIM MENDELIAN

More info about ATAXIA-TELANGIECTASIA

Medium match PUNCTATE PALMOPLANTAR KERATODERMA TYPE 1


Punctate palmoplantar keratoderma type I (PPKP1), also known as Buschke-Fischer-Brauer syndrome, is a very rare hereditary skin disease characterized by irregularly distributed epidermal hyperkeratosis of the palms and soles with wide variation among patients..

PUNCTATE PALMOPLANTAR KERATODERMA TYPE 1 Is also known as palmoplantar keratoderma, punctate type i|ppkp1|keratodermia palmoplantaris papulosa, buschke-fischer-brauer type|buschke-fischer-brauer syndrome|keratosis palmoplantaris papulosa|kppp1

Related symptoms:

  • Neoplasm
  • Pain
  • Dilatation
  • Depressivity
  • Hyperkeratosis


SOURCES: ORPHANET OMIM MENDELIAN

More info about PUNCTATE PALMOPLANTAR KERATODERMA TYPE 1

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Other less relevant matches:

Medium match NORMOSMIC CONGENITAL HYPOGONADOTROPIC HYPOGONADISM


NORMOSMIC CONGENITAL HYPOGONADOTROPIC HYPOGONADISM Is also known as isolated congenital gonadotropin deficiency|normosmic idiopathic hypogonadotropic hypogonadism|gonadotropic deficiency|nihh

Related symptoms:

  • Hypertelorism
  • Cleft palate
  • Cryptorchidism
  • Depressed nasal bridge
  • Abnormality of the dentition


SOURCES: ORPHANET MENDELIAN

More info about NORMOSMIC CONGENITAL HYPOGONADOTROPIC HYPOGONADISM

Medium match FACIAL DYSMORPHISM-DEVELOPMENTAL DELAY-BEHAVIORAL ABNORMALITIES SYNDROME DUE TO WAC POINT MUTATION


DeSanto-Shinawi syndrome is a rare neurodevelopmental disorder characterized by global developmental delay apparent in infancy or early childhood and associated with characteristic dysmorphic facial features, such as broad forehead, depressed nasal bridge with bulbous nasal tip, and deep-set eyes. Most patients also have gastrointestinal and mild ocular abnormalities, as well as behavioral problems (summary by DeSanto et al., 2015).

FACIAL DYSMORPHISM-DEVELOPMENTAL DELAY-BEHAVIORAL ABNORMALITIES SYNDROME DUE TO WAC POINT MUTATION Is also known as developmental delay, behavioral abnormalities, facial dysmorphism, and ocular abnormalities

Related symptoms:

  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Hearing impairment
  • Hypertelorism


SOURCES: OMIM ORPHANET MENDELIAN

More info about FACIAL DYSMORPHISM-DEVELOPMENTAL DELAY-BEHAVIORAL ABNORMALITIES SYNDROME DUE TO WAC POINT MUTATION

Medium match LYMPHEDEMA-DISTICHIASIS SYNDROME


Lymphedema - distichiasis is a rare syndromic lymphedema disorder characterized by lower-limb lymphedema and varying degrees of abnormal growth of eyelashes from the orifices of the Meibomian glands (distichiasis), with occasional associated manifestations.

LYMPHEDEMA-DISTICHIASIS SYNDROME Is also known as lymphedema with distichiasis

Related symptoms:

  • Muscle weakness
  • Cleft palate
  • Pain
  • Cataract
  • Ptosis


SOURCES: OMIM ORPHANET MENDELIAN

More info about LYMPHEDEMA-DISTICHIASIS SYNDROME

Low match ADNP SYNDROME


ADNP syndrome is a rare, syndromic intellectual disability characterized by intellectual disability of various severity, hypotonia, global developmental delay, severely delayed speech, behavioral problems, pain insensitivity, sleep problems, seizures, structural brain anomalies, dysmorphic features, visual problems and autism.

ADNP SYNDROME Is also known as adnp-related syndromic intellectual disability-autism spectrum disorder|hvdas|mental retardation, autosomal dominant 28|mrd28|helsmoortel-van der aa syndrome

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about ADNP SYNDROME

Low match GROWTH DELAY DUE TO INSULIN-LIKE GROWTH FACTOR I RESISTANCE


Growth delay due to IGF-I resistance is characterised by variable intrauterine and postnatal growth retardation and elevated serum IGF-I levels. Addition features include variable degrees of intellectual deficit, microcephaly and dysmorphism (broad nasal bridge and tip, smooth philtrum, thin upper and everted lower lips, short fingers, clinodactyly, wide-set nipples and pectus excavatum).

GROWTH DELAY DUE TO INSULIN-LIKE GROWTH FACTOR I RESISTANCE Is also known as igf-i resistance|resistance to igf-1|somatomedin, end-organ insensitivity to|somatomedin-c, resistance to

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about GROWTH DELAY DUE TO INSULIN-LIKE GROWTH FACTOR I RESISTANCE

Low match PITT-HOPKINS SYNDROME


Pitt-Hopkins syndrome (PHS) is characterized by the association of intellectual deficit, characteristic facial dysmorphism and problems of abnormal and irregular breathing.

PITT-HOPKINS SYNDROME Is also known as encephalopathy, severe epileptic, with autonomic dysfunction|mental retardation, syndromal, with intermittent hyperventilation

Related symptoms:

  • Intellectual disability
  • Seizures
  • Global developmental delay
  • Generalized hypotonia
  • Hearing impairment


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about PITT-HOPKINS SYNDROME

Low match ACROMEGALY


Acromegaly is an acquired disorder related to excessive production of growth hormone (GH) and characterized by progressive somatic disfigurement (mainly involving the face and extremities) and systemic manifestations.

Related symptoms:

  • Neoplasm
  • Hypertension
  • Fatigue
  • Frontal bossing
  • Abnormality of the dentition


SOURCES: ORPHANET MENDELIAN

More info about ACROMEGALY

Top 5 symptoms//phenotypes associated to Breast carcinoma and Anxiety

Symptoms // Phenotype % cases
Seizures Uncommon - Between 30% and 50% cases
Strabismus Uncommon - Between 30% and 50% cases
Intellectual disability Uncommon - Between 30% and 50% cases
Microcephaly Uncommon - Between 30% and 50% cases
Abnormal facial shape Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Breast carcinoma and Anxiety. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Depressivity Generalized hypotonia Global developmental delay Depressed nasal bridge Diabetes mellitus Neoplasm Synophrys Broad forehead Deeply set eye Full cheeks Thin upper lip vermilion Obesity Coarse facial features Failure to thrive Short stature Hypoplasia of the corpus callosum Feeding difficulties Wide intermamillary distance Cryptorchidism Hypertelorism Hodgkin lymphoma Wide nasal bridge Astigmatism Carcinoma Small hand Widely spaced teeth Attention deficit hyperactivity disorder Fatigue Neurological speech impairment Thick lower lip vermilion Paresthesia Constipation Muscular hypotonia

Rare Symptoms - Less than 30% cases


Pain Micropenis Hearing impairment Postnatal growth retardation Finger clinodactyly Impotence Gynecomastia Telangiectasia Cafe-au-lait spot Truncal ataxia Cerebral palsy Multiple cafe-au-lait spots Epidermal acanthosis Delayed skeletal maturation Abnormality of the dentition Female hypogonadism Upslanted palpebral fissure Mandibular prognathia Tapered finger Cleft palate Sleep apnea Thickened skin Acanthosis nigricans Autism Delayed speech and language development Smooth philtrum Gastroesophageal reflux Low-set ears Webbed neck Growth hormone deficiency Muscular hypotonia of the trunk Abnormality of cardiovascular system morphology Ptosis Cataract Inverted nipples Agitation Autistic behavior Hirsutism Myopia Thick eyebrow Lymphoma Abnormality of the pinna Aggressive behavior Sparse scalp hair Hyperactivity Growth delay Prominent forehead Motor delay Short neck Absent speech Clinodactyly Type II diabetes mellitus Sleep disturbance Ataxia Pneumonia Flexion contracture Behavioral abnormality Abnormality of the liver Muscle weakness Gait ataxia Hepatocellular carcinoma Gait disturbance Neoplasm of the pancreas Scoliosis Recurrent infections Colon cancer Dysarthria Visual impairment Migraine Hypertonia Cognitive impairment Delayed puberty Reduced subcutaneous adipose tissue Truncal obesity Chorea Delayed cranial suture closure High pitched voice Radial deviation of finger Lipodystrophy Patent foramen ovale Sandal gap Accelerated skeletal maturation Decreased body weight Pterygium Small face Severe intrauterine growth retardation Increased serum insulin-like growth factor 1 Intellectual disability, moderate Pes planus Pes cavus Encephalopathy Intellectual disability, severe Anteverted nares Talipes equinovarus Abnormality of the skeletal system Burkitt lymphoma Severe failure to thrive Hypoplastic facial bones Prominent scalp veins Rieger anomaly Broad finger Esodeviation Perimembranous ventricular septal defect Abnormality of the rib cage Broad nasal tip Maternal diabetes Blue sclerae Highly arched eyebrow Triangular face Exotropia Eyelid coloboma Long palpebral fissure Narrow nasal bridge Obsessive-compulsive behavior Language impairment Bilateral ptosis Abnormal pyramidal sign Plagiocephaly Cerebral visual impairment Amblyopia Juvenile cataract Stereotypy Broad thumb Malabsorption Nausea and vomiting Dyskinesia Iris coloboma Joint hypermobility Hypermetropia Microtia Generalized neonatal hypotonia Microtia, first degree Delayed eruption of teeth Narrow mouth Short foot Protruding ear Everted lower lip vermilion Inability to walk Short distal phalanx of finger Short palm Thin vermilion border Small for gestational age Retrognathia Abdominal pain Irritability Severe short stature Weight loss Pectus excavatum Malar flattening Long philtrum Ventricular septal defect Intrauterine growth retardation Developmental regression High palate Micrognathia Apnea Thick vermilion border Wide mouth Long face Growth abnormality Abnormality of the fingernails Generalized hirsutism Hoarse voice Tall stature Mitral regurgitation Osteoarthritis Macroglossia Wide nose Hypertrophic cardiomyopathy Large hands Arthralgia Macrotia Hyperhidrosis Kyphosis Frontal bossing Hypertension Overhanging nasal tip Triangular nasal tip Broad fingertip Acne Generalized hyperpigmentation Narrow foot Long penis Abnormality of reproductive system physiology Broad jaw Macrodactyly Dysmenorrhea Pituitary prolactin cell adenoma Deep plantar creases Galactorrhea Hypersomnia Paraganglioma Pheochromocytoma Spinal canal stenosis Anterior hypopituitarism Deep palmar crease Neoplasm of the endocrine system Dysuria Abnormality of the endocrine system Abnormal toenail morphology Broad foot Growth hormone excess Joint swelling Palpebral edema Intermittent hyperventilation Failure of eruption of permanent teeth Short philtrum Narrow forehead Hypopigmented skin patches Mutism Aplasia/Hypoplasia of the corpus callosum Abnormal palate morphology Intellectual disability, progressive Abnormal autonomic nervous system physiology Postnatal microcephaly Aganglionic megacolon Open mouth Cyanosis Incoordination Specific learning disability Convex nasal ridge Prominent nose Abdominal distention Hypopigmentation of the skin Single transverse palmar crease Gastrointestinal hemorrhage Severe global developmental delay Prominent nasal bridge Coarse hair Short metatarsal Small cerebral cortex Echolalia Square face Large beaked nose Happy demeanor Pes valgus Abnormal pattern of respiration Thickened helices Breathing dysregulation Abnormality of the helix Clubbing of fingers Misalignment of teeth Self-injurious behavior Esophagitis Acrocyanosis Hiatus hernia Hyperventilation Dysphasia Aphasia Supernumerary nipple Overlapping toe Cupped ear Clubbing Coloboma Abnormal heart morphology Memory impairment Leukemia Interosseus muscle atrophy Decreased/absent ankle reflexes Immunoglobulin IgG2 deficiency Progressive spinal muscular atrophy Non-Hodgkin lymphoma Mucosal telangiectasiae Aplasia/Hypoplasia of the thymus Increased sensitivity to ionizing radiation Chronic hepatitis Defective B cell differentiation Decreased proportion of CD4-positive T cells Elevated alpha-fetoprotein Abnormal spermatogenesis Neoplasm of the breast Chronic myelogenous leukemia Conjunctival telangiectasia Abnormality of chromosome stability Cellular immunodeficiency Chronic lymphatic leukemia IgE deficiency Distal muscle weakness Absent Achilles reflex Hypergranulosis Camptodactyly Osteopenia Osteoporosis Recurrent respiratory infections Myoclonus Difficulty walking Elevated hepatic transaminase Transitional cell carcinoma of the bladder Orthokeratosis Parakeratosis Dilatation Renal cell carcinoma Squamous cell carcinoma Scaling skin Abnormality of the nail Respiratory tract infection Abnormality of the skin Palmoplantar keratoderma Papule Hyperkeratosis Hypoplasia of the thymus Spinocerebellar tract degeneration Decreased testicular size Distal amyotrophy Abnormality of movement Reduced tendon reflexes Oculomotor apraxia Recurrent pneumonia Unsteady gait Abnormality of the hair Lymphopenia Abnormal vertebral morphology Sinusitis Limb ataxia Polycystic ovaries Bronchiectasis Polyneuropathy Choreoathetosis Intention tremor Pancytopenia Abnormal cerebellum morphology Apraxia Hepatitis Decreased antibody level in blood Slurred speech Spinal muscular atrophy Lymphoproliferative disorder IgA deficiency Abnormality of the testis B-cell lymphoma Renal neoplasm Recurrent bronchitis Chromosome breakage Recurrent lower respiratory tract infections Severe combined immunodeficiency Acute lymphoblastic leukemia Hypopigmentation of hair Prematurely aged appearance Athetosis Myeloid leukemia Abnormality of the immune system Telangiectasia of the skin Abnormality of eye movement Aplasia/Hypoplasia of the skin Resting tremor Premature graying of hair Combined immunodeficiency Glucose intolerance Immunodeficiency Primary amenorrhea Joint laxity Recurrent urinary tract infections Tubulointerstitial nephritis Overweight Glomerulopathy Cellulitis Ectropion Recurrent skin infections Conjunctivitis Lymphedema Neuroblastoma Varicose veins Bruising susceptibility Cleft upper lip Proteinuria Photophobia Hypogonadism Arrhythmia Patent ductus arteriosus Ovarian neoplasm Edema Corneal erosion Venous insufficiency Intestinal polyposis Respiratory distress Neonatal hypotonia Hallucinations Increased intracranial pressure Inguinal hernia Progressive cerebellar ataxia Hernia Hemiplegia/hemiparesis Short nose Atrial septal defect Downslanted palpebral fissures Distichiasis Basal cell carcinoma Visual field defect Lipedema Spinalarachnoid cyst Abnormality of the pulmonary vasculature Predominantly lower limb lymphedema Fibrosarcoma Knee pain Renal duplication Pituitary adenoma Prostate cancer Dystonia Decreased serum testosterone level Increased female libido Abnormality of body height Absence of pubertal development Non-obstructive azoospermia Hypoplasia of the ovary Eunuchoid habitus Decreased testosterone in males Breast hypoplasia Absence of secondary sex characteristics Male hypogonadism Skeletal muscle atrophy Generalized joint laxity Secondary amenorrhea Sparse body hair Hypoplasia of the uterus Cerebellar atrophy Congenital sensorineural hearing impairment Abnormality of the voice Azoospermia Hypogonadotrophic hypogonadism Tremor Peripheral neuropathy Dysgraphia Neoplasm of the skeletal system Amaurosis fugax Downturned corners of mouth Leiomyosarcoma Pancreatic adenocarcinoma Bulbous nose Glioblastoma multiforme Agnosia Neoplasm of the thyroid gland Benign neoplasm of the central nervous system Abnormality of creatine metabolism Sensorineural hearing impairment Neoplasm of the rectum Cardiac diverticulum Urinary tract neoplasm Brachycephaly Posteriorly rotated ears Midface retrusion Nystagmus Spasticity Anemia Cortical diaphyseal thickening of the upper limbs



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Ventricular septal defect and Thin upper lip vermilion, related diseases and genetic alterations Lymphoma and Depressivity, related diseases and genetic alterations Obesity and Skeletal muscle atrophy, related diseases and genetic alterations Strabismus and Delayed eruption of teeth, related diseases and genetic alterations

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