Carcinoma, and Bronchiectasis

Diseases related with Carcinoma and Bronchiectasis

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


Top matches:

High match IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2


IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2 Is also known as antibody deficiency due to taci defect|hypogammaglobulinemia due to taci deficiency

Related symptoms:

  • Neoplasm
  • Hepatomegaly
  • Diarrhea
  • Splenomegaly
  • Immunodeficiency


SOURCES: OMIM MENDELIAN

More info about IMMUNODEFICIENCY, COMMON VARIABLE, 2; CVID2

High match ALPHA-1-ANTITRYPSIN DEFICIENCY


Alpha-1-antitrypsin deficiency is a hereditary disease that develops in adulthood and is characterized by chronic liver disorders (cirrhosis), respiratory disorders (emphysema), and rarely panniculitis.

ALPHA-1-ANTITRYPSIN DEFICIENCY Is also known as deficiency in alpa-1-proteinase inhibitor

Related symptoms:

  • Neoplasm
  • Hypertension
  • Hepatomegaly
  • Fatigue
  • Respiratory distress


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about ALPHA-1-ANTITRYPSIN DEFICIENCY

High match IDIOPATHIC PULMONARY FIBROSIS


Idiopathic pulmonary fibrosis (IPF) is a nonneoplastic pulmonary disease that is characterized by the formation of scar tissue within the lungs in the absence of any known cause.

IDIOPATHIC PULMONARY FIBROSIS Is also known as cfa|uip|usual interstitial pneumonia|interstitial pneumonitis, usual|idiopathic pulmonary fibrosis, familial|cryptogenic fibrosing alveolitis|fibrosing alveolitis, cryptogenic|fibrocystic pulmonary dysplasia

Related symptoms:

  • Neoplasm
  • Hypertension
  • Fever
  • Respiratory insufficiency
  • Respiratory distress


SOURCES: OMIM ORPHANET MENDELIAN

More info about IDIOPATHIC PULMONARY FIBROSIS

Mendelian

Too many results?
We can help you with your rare disease diagnosis.

Learn more

Other less relevant matches:

High match WHIM SYNDROME


WHIM (warts, hypogammaglobulinemia, infections, and myelokathexis) syndrome is a congenital autosomal dominant immune deficiency characterized by abnormal retention of mature neutrophils in the bone marrow (myelokathexis) and occasional hypogammaglobulinemia, associated with an increased risk for bacterial infections and a susceptibility to human papillomavirus (HPV) induced lesions (cutaneous warts, genital dysplasia and invasive mucosal carcinoma).

WHIM SYNDROME Is also known as warts, hypogammaglobulinemia, infections, and myelokathexis syndrome|warts-infections-leukopenia-myelokatexis syndrome|wilm|warts-hypogammaglobulinemia-infections-myelokathexis syndrome

Related symptoms:

  • Hearing impairment
  • Neoplasm
  • Fever
  • Congestive heart failure
  • Immunodeficiency


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about WHIM SYNDROME

High match AUTOIMMUNE ENTEROPATHY AND ENDOCRINOPATHY-SUSCEPTIBILITY TO CHRONIC INFECTIONS SYNDROME


Autoimmune enteropathy and endocrinopathy-susceptibility to chronic infections syndrome is an extremely rare, autosomal dominant immunological disorder characterized by variable enteropathy, endocrine disorders (e.g. type 1 diabetes mellitus, hypothyroidism), immune dysregulation with pulmonary and blood-borne bacterial infections, and fungal infections (chronic mucocutaneous candidiasis) developing in infancy. Other manifestations include short stature, eczema, hepatosplenomegaly, delayed puberty, and osteoporosis/osteopenia.

AUTOIMMUNE ENTEROPATHY AND ENDOCRINOPATHY-SUSCEPTIBILITY TO CHRONIC INFECTIONS SYNDROME Is also known as candf7|candidiasis, familial, 7|candidiasis, familial chronic mucocutaneous, autosomal dominant

Related symptoms:

  • Global developmental delay
  • Short stature
  • Growth delay
  • Anemia
  • Diarrhea


SOURCES: ORPHANET OMIM MENDELIAN

More info about AUTOIMMUNE ENTEROPATHY AND ENDOCRINOPATHY-SUSCEPTIBILITY TO CHRONIC INFECTIONS SYNDROME

High match CYSTIC FIBROSIS


Cystic fibrosis (CF) is a genetic disorder characterized by the production of sweat with a high salt content and mucus secretions with an abnormal viscosity.

CYSTIC FIBROSIS Is also known as mucoviscidosis|cf

Related symptoms:

  • Growth delay
  • Neoplasm
  • Failure to thrive
  • Pain
  • Hypertension


SOURCES: ORPHANET OMIM MENDELIAN

More info about CYSTIC FIBROSIS

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

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

Medium match KEUTEL SYNDROME


Keutel syndrome is characterised by diffuse cartilage calcification, brachytelephalangism, peripheral pulmonary artery stenoses and facial dysmorphism.

KEUTEL SYNDROME Is also known as pulmonic stenosis-brachytelephalangism-calcification of cartilages syndrome|pulmonic stenosis, brachytelephalangism, and calcification of cartilages

Related symptoms:

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


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about KEUTEL SYNDROME

Medium match COSTELLO SYNDROME


Costello syndrome (CS) is a rare multisystemic disorder characterized by failure to thrive, short stature, developmental delay or intellectual disability, joint laxity, soft skin, and distinctive facial features. Cardiac and neurological involvement is common and there is an increased lifetime risk of certain tumors.

COSTELLO SYNDROME Is also known as fcs syndrome|faciocutaneoskeletal syndrome

Related symptoms:

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


SOURCES: MESH OMIM ORPHANET MENDELIAN

More info about COSTELLO SYNDROME

Top 5 symptoms//phenotypes associated to Carcinoma and Bronchiectasis

Symptoms // Phenotype % cases
Neoplasm Common - Between 50% and 80% cases
Immunodeficiency Common - Between 50% and 80% cases
Hypertension Common - Between 50% and 80% cases
Respiratory tract infection Uncommon - Between 30% and 50% cases
Respiratory failure Uncommon - Between 30% and 50% cases
Mendelian

Accelerate your rare disease diagnosis with us

Learn more

Other less frequent symptoms

Patients with Carcinoma and Bronchiectasis. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Pneumonia Short stature Decreased antibody level in blood Recurrent infections Hepatomegaly Lymphoma Growth delay Failure to thrive Dilatation Intellectual disability Recurrent respiratory infections Sinusitis Delayed puberty Diarrhea Portal hypertension Chronic obstructive pulmonary disease Congestive heart failure B-cell lymphoma Gastroesophageal reflux Respiratory insufficiency Delayed skeletal maturation Pulmonary arterial hypertension Lymphopenia Cognitive impairment Diabetes mellitus Strabismus Abnormal lung morphology Scoliosis Anemia Seizures Global developmental delay Recurrent upper respiratory tract infections Emphysema Elevated hepatic transaminase Hepatitis Recurrent bronchitis Cirrhosis Otitis media Depressed nasal bridge Abnormality of the liver Respiratory distress Recurrent pneumonia

Rare Symptoms - Less than 30% cases


Exocrine pancreatic insufficiency Obstructive lung disease Myopia Abnormality of chromosome stability Epicanthus Thrombocytopenia Low-set, posteriorly rotated ears Muscular hypotonia Osteopenia Malabsorption Infertility Asthma Cutis laxa Non-Hodgkin lymphoma Hodgkin lymphoma Wide nose Abnormality of the skeletal system Eczema Anteverted nares Abnormality of the pancreas Joint laxity Macrotia Pneumothorax Pectus carinatum Arthrogryposis multiplex congenita Hypotrichosis Joint hyperflexibility Aortic aneurysm Severe short stature Sepsis Alopecia Joint hypermobility Cellular immunodeficiency Abnormality of the testis Cardiomyopathy Short neck Postural instability Sparse hair Verrucae Neutropenia IgA deficiency Hepatocellular carcinoma Nystagmus Apraxia Recurrent sinusitis Cafe-au-lait spot Thyroiditis IgG deficiency Dysarthria Abnormal facial shape Pulmonary fibrosis Clubbing Large face Leukemia Reduced tendon reflexes Cough Recurrent bacterial infections Hemoptysis Fever Dyspnea Pulmonic stenosis Combined immunodeficiency Splenomegaly Autoimmunity Abnormality of the hair Recurrent otitis media Ventricular septal defect Meningitis Osteoporosis Wheezing Hearing impairment Intellectual disability, mild Scarring Hypogonadism Low-set ears Abnormality of the dentition Cerebral cortical atrophy Hyperkeratosis Proptosis Polyhydramnios Ptosis Cryptorchidism Micrognathia Hypertelorism Generalized hypotonia Cartilaginous ossification of larynx Hyperhidrosis Inguinal hernia High palate Abnormality of cardiovascular system morphology Myopathy Edema Atrial septal defect Hydrocephalus Long philtrum Ventriculomegaly Talipes equinovarus Dysphagia Cartilaginous ossification of nose Renal insufficiency Cerebral atrophy Absent speech Feeding difficulties Hernia Frontal bossing Pectus excavatum Downslanted palpebral fissures Arrhythmia Macrocephaly Abnormal heart morphology Motor delay Short nose Pes cavus Delayed speech and language development Posteriorly rotated ears Premature fusion of phalangeal epiphyses Deep philtrum Calcification of the auricular cartilage Long fibula Midface retrusion Malar flattening Optic atrophy 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 Narrow vertebral interpedicular distance Long face Abnormality of the distal phalanx of finger Abnormal T cell morphology Hypoplastic anemia Abnormally ossified vertebrae Abnormal bone ossification Neonatal short-limb short stature Congenital hypoplastic anemia Spinal dysraphism Hypersplenism Normocytic anemia Mucopolysacchariduria Abnormal diaphysis morphology Diaphyseal thickening Bronchiolitis Hydronephrosis Short distal phalanx of finger Costal cartilage calcification Pulmonary artery stenosis Soft, doughy skin Tracheal atresia Calcification of cartilage Arterial calcification Pulmonary artery hypoplasia Abdominal aortic aneurysm Papillary thyroid carcinoma Short nail Shortening of all distal phalanges of the fingers Peripheral pulmonary artery stenosis Thyroid carcinoma Short hallux Chronic sinusitis Irregular vertebral endplates Underdeveloped nasal alae Epiphyseal stippling Mixed hearing impairment Nasal speech Dermal atrophy Coarse facial features Growth abnormality Progressive hearing impairment Spontaneous abortion Leukodystrophy Short thumb Short phalanx of finger Sloping forehead Cerebral calcification Memory impairment Kyphoscoliosis Long eyelashes Hypoglycemia Hyperextensibility of the finger joints Asymmetric septal hypertrophy Abnormal mitral valve morphology Broad philtrum Fasting hypoglycemia Hypoplasia of teeth Concave nail Rhabdomyosarcoma Labial hypoplasia Broad femoral neck Schwannoma Abnormality of earlobe Limited elbow movement Fetal distress Bronchomalacia Deep palmar crease Redundant neck skin Thin nail Megalencephaly Soft skin Obstructive sleep apnea Severe postnatal growth retardation Microscopic hematuria Thickened nuchal skin fold Fragile nails Barrel-shaped chest Lack of skin elasticity Progeroid facial appearance Woolly hair Large earlobe Thick upper lip vermilion Achilles tendon contracture Large forehead Central apnea Papilloma Deep plantar creases Arnold-Chiari type I malformation Enlarged cerebellum Neonatal sepsis Choroid plexus papilloma Bladder carcinoma Cardiomyocyte hypertrophy Loose anagen hair Macrocephaly at birth Myofiber disarray Embryonal rhabdomyosarcoma Vitreomacular adhesion Tendon rupture Alveolar rhabdomyosarcoma Lymphangiectasis Congenital neuroblastoma Thickened Achilles tendon Systolic heart murmur Multifocal atrial tachycardia Deep-set nails Hematemesis Ulnar deviation of the wrist Melena Triangular mouth Capillary malformation Bladder neoplasm Abnormal pulmonary valve morphology Duodenal ulcer Body odor Vestibular Schwannoma Postprandial hyperglycemia Shyness Hypopnea Concentric hypertrophic cardiomyopathy Transitional cell carcinoma of the bladder Ganglioneuroblastoma Frontal hirsutism Neonatal hypoglycemia Syringomyelia Abnormality of the nervous system Mitral valve prolapse Premature birth Webbed neck Growth hormone deficiency Abnormality of the skin Hip dysplasia Overgrowth Epidermal acanthosis Full cheeks Thick lower lip vermilion Atrial fibrillation Hypoplasia of dental enamel Decreased body weight Metaphyseal chondrodysplasia Hyperpigmentation of the skin Nevus Macroglossia Lymphedema Wide mouth Hypertrophic cardiomyopathy Intellectual disability, moderate Apnea Feeding difficulties in infancy Irritability Postnatal growth retardation Hypermetropia Tetraplegia Astigmatism Tachycardia Thick vermilion border Hematuria High, narrow palate Sleep disturbance Ascites Wide anterior fontanel Hydrops fetalis Central hypotonia Neurodevelopmental delay Hyperglycemia Bilateral cryptorchidism Hypoplastic toenails Tricuspid regurgitation Rocker bottom foot Large for gestational age Reduced subcutaneous adipose tissue Pleural effusion Keratoconus Curly hair Neuroblastoma Rhabdomyolysis Ulnar deviation of finger Generalized hyperpigmentation Tracheomalacia Heart murmur Failure to thrive in infancy Hoarse voice Abnormal dermatoglyphics Pointed chin Narrow palate Abnormality of dental enamel Short chin Abnormality of the fingernails Acanthosis nigricans Infantile muscular hypotonia Redundant skin Hemangioma Arnold-Chiari malformation Relative macrocephaly Laryngomalacia Poor suck Hyperextensible skin Pyloric stenosis Metaphyseal cupping Short palm Aplasia/Hypoplasia affecting the eye Medial calcification of large arteries Tachypnea Azoospermia Pancreatitis Nephrocalcinosis Insulin resistance Dehydration Abdominal distention Dyskinesia Nausea Abdominal pain Vomiting Pain Abnormal serum interferon-gamma level Esophageal carcinoma Intestinal obstruction Oropharyngeal squamous cell carcinoma Susceptibility to herpesvirus Recurrent Aspergillus infections Carotid artery dilatation Functional abnormality of the bladder Autoimmune neutropenia Renal artery stenosis Renovascular hypertension Antiphospholipid antibody positivity B lymphocytopenia Primary hypothyroidism Decrease in T cell count Enterocolitis Immune dysregulation Hypercalciuria Malnutrition Villous atrophy Meconium ileus Peripheral neuropathy Flexion contracture Spasticity Muscle weakness Ataxia Microcephaly Microscopic nephrocalcinosis Echogenic fetal bowel Cellular metachromasia Biliary tract obstruction Elevated sweat chloride Absent vas deferens Obstructive azoospermia Recurrent bronchopulmonary infections Pancreatic adenocarcinoma Steatorrhea Productive cough Secretory diarrhea Chronic pancreatitis Chronic infection Nasal polyposis Rectal prolapse Ileus Biliary cirrhosis Allergy Cor pulmonale Chronic lung disease Neoplasm of the pancreas Bronchitis Male infertility Generalized osteoporosis Chronic mucocutaneous candidiasis Tremor Cyanosis Honeycomb lung Reticular pattern on pulmonary HRCT Hypocapnia Alveolar cell carcinoma Crackles Pulmonary insufficiency Right ventricular failure Clubbing of fingers Pulmonary infiltrates Polycythemia Exertional dyspnea Interstitial pulmonary abnormality Increased antibody level in blood Scaling skin Panniculitis Arthritis Neoplasm of the liver Vasculitis Cholestasis Nephrotic syndrome Hepatic failure Jaundice Weight loss Fatigue Gastrointestinal carcinoma Follicular hyperplasia Impaired T cell function IgM deficiency Recurrent sinopulmonary infections Conjunctivitis Ground-glass opacification on pulmonary HRCT Carious teeth Abnormality of the endocrine system Hepatosplenomegaly Dilatation of the cerebral artery Hashimoto thyroiditis Pulmonary embolism Autoimmune thrombocytopenia Autoimmune hemolytic anemia Inflammation of the large intestine Patent foramen ovale Encephalitis Leukoencephalopathy Abnormal intestine morphology Purpura Type I diabetes mellitus Inflammatory abnormality of the skin Hemolytic anemia Hypothyroidism Recurrent urinary tract infections Myelokathexis Bone marrow hypercellularity Hypersegmentation of neutrophil nuclei Tonsillitis Septic arthritis Folliculitis Abnormality of bone marrow cell morphology Abnormality of female external genitalia Abnormality of female internal genitalia Atelectasis Periodontitis Cellulitis Osteomyelitis Leukocytosis Skeletal muscle atrophy Gait disturbance Aplasia/Hypoplasia of the abdominal wall musculature Lumbar hyperlordosis Short ribs Sparse and thin eyebrow Gingival overgrowth Abnormality of retinal pigmentation Rhizomelia Abnormality of epiphysis morphology Aganglionic megacolon Bowing of the long bones Abnormal form of the vertebral bodies Abnormality of the metaphysis Depressed nasal ridge Fine hair Blue sclerae Abnormality of the ribs Sparse eyelashes Convex nasal ridge Gastrointestinal hemorrhage Hypopigmentation of the skin Small hand Micromelia Narrow chest Abnormal cardiac septum morphology Hyperlordosis EEG abnormality Skeletal dysplasia Brachycephaly Prominent forehead Constipation Wide nasal bridge Hypocalcemia Accelerated skeletal maturation Defective B cell differentiation High hypermetropia Aplastic anemia Generalized joint laxity Tracheal stenosis Fair hair Heart block Upper limb undergrowth Overweight Thrombocytosis Distal arthrogryposis Esophageal atresia Hypoplasia of the odontoid process Anal stenosis Macrocytic anemia Metaphyseal dysplasia Abnormality of the hip bone Neoplasm of the skin Tibial bowing Basal cell carcinoma Limited elbow extension Femoral bowing Mesomelia Short thorax Squamous cell carcinoma Cone-shaped epiphysis Metaphyseal widening Genu varum Abnormality of pelvic girdle bone morphology Disproportionate short-limb short stature Sacral dimple Abnormal palate morphology Visual impairment IgE deficiency Cerebellar atrophy Type II diabetes mellitus Athetosis Spinal muscular atrophy Polycystic ovaries Slurred speech Breast carcinoma Cerebral palsy Oculomotor apraxia Truncal ataxia Abnormal vertebral morphology Limb ataxia Telangiectasia Choreoathetosis Intention tremor Pancytopenia Chorea Premature graying of hair Progressive cerebellar ataxia Abnormal cerebellum morphology Polyneuropathy Distal amyotrophy Unsteady gait Abnormality of movement Abnormality of eye movement Neurological speech impairment Distal muscle weakness Anxiety Difficulty walking Gait ataxia Myoclonus Dystonia Glucose intolerance Resting tremor Interosseus muscle atrophy Chronic lymphatic leukemia Decreased/absent ankle reflexes Immunoglobulin IgG2 deficiency Progressive spinal muscular atrophy Mucosal telangiectasiae Aplasia/Hypoplasia of the thymus Increased sensitivity to ionizing radiation Female hypogonadism Chronic hepatitis Decreased proportion of CD4-positive T cells Elevated alpha-fetoprotein Abnormal spermatogenesis Neoplasm of the breast Chronic myelogenous leukemia Conjunctival telangiectasia Hypoplasia of the thymus Aplasia/Hypoplasia of the skin Absent Achilles reflex Spinocerebellar tract degeneration Lymphoproliferative disorder Renal neoplasm Chromosome breakage Recurrent lower respiratory tract infections Severe combined immunodeficiency Acute lymphoblastic leukemia Hypopigmentation of hair Prematurely aged appearance Myeloid leukemia Abnormality of the immune system Telangiectasia of the skin Multiple cafe-au-lait spots Increased corneal curvature



If you liked this article maybe you will also find interesting the following in-depth articles about other rare diseases, like Macrocephaly and Cholestasis, related diseases and genetic alterations Brachydactyly and Round face, related diseases and genetic alterations Cognitive impairment and Apraxia, related diseases and genetic alterations Sensorineural hearing impairment and Pectus carinatum, related diseases and genetic alterations Ataxia and Muscular dystrophy, related diseases and genetic alterations Microcephaly and Proteinuria, related diseases and genetic alterations

Need help with a diagnosis?

Learn more about how to achieve it with Mendelian


Learn more