Carcinoma, and Erythema

Diseases related with Carcinoma and Erythema

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


Top matches:

High match PORPHYRIA CUTANEA TARDA


Porphyria cutanea tarda (PCT) is characterized by light-sensitive dermatitis and the excretion of large amounts of uroporphyrin in urine (Elder et al., 1980).De Verneuil et al. (1978) and others classified porphyria cutanea tarda, the most common type of porphyria, into 2 types: type I (OMIM ), or 'sporadic' type, associated with approximately 50% level of uroporphyrinogen decarboxylase (UROD) in liver (Elder et al., 1978; Felsher et al., 1982), and type II, or 'familial' type, characterized by 50% deficient activity of the same enzyme in many tissues (Kushner et al., 1976; Elder et al., 1980).PCT type II is an autosomal dominant disorder with low penetrance and constitutes about 20% of cases of PCT. Recognized exacerbating factors of PCT include iron overload, excessive use of alcohol, exposure to polyhalogenated aromatic chemicals, exposure to estrogens, chronic viral hepatitis C, HIV infections, and mutation in the HFE gene (OMIM ) that are responsible for hereditary hemochromatosis (OMIM ) (review by Lambrecht et al., 2007).

PORPHYRIA CUTANEA TARDA Is also known as uroporphyrinogen decarboxylase deficiency|pct|pct, type ii|pct, 'familial' type|urod deficiency|porphyria cutanea tarda, type ii|porphyria, hepatocutaneous type

Related symptoms:

  • Anemia
  • Edema
  • Alopecia
  • Carcinoma
  • Erythema


SOURCES: OMIM ORPHANET MENDELIAN

More info about PORPHYRIA CUTANEA TARDA

High match PAPILLON-LEFÈVRE SYNDROME


Papillon-Lefèvre syndrome (PLS) is a rare ectodermal dysplasia characterized by palmoplantar keratoderma associated with early-onset periodontitis.

PAPILLON-LEFÈVRE SYNDROME Is also known as keratosis palmoplantar-periodontopathy syndrome|pls|keratosis palmoplantaris with periodontopathia

Related symptoms:

  • Intellectual disability
  • Neoplasm
  • Abnormality of the dentition
  • Recurrent respiratory infections
  • Hyperhidrosis


SOURCES: OMIM ORPHANET MESH MENDELIAN

More info about PAPILLON-LEFÈVRE SYNDROME

High match MULTIPLE ENDOCRINE NEOPLASIA TYPE 1


Multiple endocrine neoplasia Type 1 (MEN1) is a frequent form of MEN (see this term), a rare inherited cancer syndrome, characterized by the development of neuroendocrine tumors of the parathyroid, pancreas, and anterior pituitary gland, and less commonly the adrenal cortical gland, with other non-endocrine tumors in some patients.

MULTIPLE ENDOCRINE NEOPLASIA TYPE 1 Is also known as men1|wermer syndrome|endocrine adenomatosis, multiple|mea i|men i

Related symptoms:

  • Seizures
  • Neoplasm
  • Pain
  • Vomiting
  • Diarrhea


SOURCES: OMIM ORPHANET MENDELIAN

More info about MULTIPLE ENDOCRINE NEOPLASIA TYPE 1

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High match MULTIPLE ENDOCRINE NEOPLASIA TYPE 4


Multiple endocrine neoplasia type 4 (MEN4) is a very rare form of MEN (see this term), an inherited cancer syndrome, characterized by parathyroid and anterior pituitary tumors, possibly associated with adrenal, renal, and reproductive organ tumors.

MULTIPLE ENDOCRINE NEOPLASIA TYPE 4 Is also known as men4

Related symptoms:

  • Neoplasm
  • Hypertension
  • Diarrhea
  • Diabetes mellitus
  • Hypothyroidism


SOURCES: OMIM MESH ORPHANET MENDELIAN

More info about MULTIPLE ENDOCRINE NEOPLASIA TYPE 4

High match BENIGN CHRONIC PEMPHIGUS; BCPM


Hailey-Hailey disease, also known as benign chronic pemphigus, is a rare autosomal dominant cutaneous disorder that usually becomes manifest in the third or fourth decade of life with erythema, vesicles, and erosions involving the body folds, particularly the groin and axillary regions. Other sites of the body, such as the neck, perianal, and submammary regions, may likewise be affected (summary by Poblete-Gutierrez et al., 2004).This disorder was first described by the dermatologist brothers Hailey and Hailey (1939).

BENIGN CHRONIC PEMPHIGUS; BCPM Is also known as hhd|hailey-hailey disease|pemphigus, benign familial

Related symptoms:

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


SOURCES: OMIM MENDELIAN

More info about BENIGN CHRONIC PEMPHIGUS; BCPM

High match MUTILATING PALMOPLANTAR KERATODERMA WITH PERIORIFICIAL KERATOTIC PLAQUES


Mutilating palmoplantar keratoderma (PPK) with periorificial keratotic plaques (also known as Olmsted syndrome) is a hereditary palmoplantar keratoderma characterized by the combination of bilateral mutilating transgredient palmoplantar keratoderma and periorificial keratotic plaques.

MUTILATING PALMOPLANTAR KERATODERMA WITH PERIORIFICIAL KERATOTIC PLAQUES Is also known as palmoplantar and periorificial keratoderma|mutilating palmoplantar hyperkeratosis with periorificial keratotic plaques|olms|olmsted syndrome

Related symptoms:

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


SOURCES: ORPHANET OMIM MENDELIAN

More info about MUTILATING PALMOPLANTAR KERATODERMA WITH PERIORIFICIAL KERATOTIC PLAQUES

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 KINDLER SYNDROME


Kindler syndrome (KS) is the fourth major type of epidermolysis bullosa (EB), besides simplex, junctional and dystrophic forms, and is characterized by skin fragility and blistering at birth followed by development of photosensitivity and progressive poikilodermatous skin changes.

KINDLER SYNDROME Is also known as poikiloderma, hereditary acrokeratotic|poikiloderma of kindler|poikiloderma, congenital, with bullae, weary type|bullous acrokeratotic poikiloderma of kindler and weary|ks

Related symptoms:

  • Anemia
  • Flexion contracture
  • Dysphagia
  • Syndactyly
  • Hyperkeratosis


SOURCES: OMIM ORPHANET MENDELIAN

More info about KINDLER SYNDROME

High match XERODERMA PIGMENTOSUM


Xeroderma pigmentosum (XP) is a rare genodermatosis characterized by extreme sensitivity to ultraviolet (UV)-induced changes in the skin and eyes, and multiple skin cancers. It is subdivided into 8 complementation groups, according to the affected gene: classical XP (XPA to XPG) and XP variant (XPV) (see these terms).

XERODERMA PIGMENTOSUM Is also known as xeroderma pigmentosum i|xp1|xp, group a|xp

Related symptoms:

  • Intellectual disability
  • Seizures
  • Short stature
  • Hearing impairment
  • Microcephaly


SOURCES: OMIM ORPHANET MENDELIAN

More info about XERODERMA PIGMENTOSUM

Top 5 symptoms//phenotypes associated to Carcinoma and Erythema

Symptoms // Phenotype % cases
Squamous cell carcinoma Common - Between 50% and 80% cases
Neoplasm Common - Between 50% and 80% cases
Hyperkeratosis Common - Between 50% and 80% cases
Alopecia Uncommon - Between 30% and 50% cases
Intellectual disability Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

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

Uncommon Symptoms - Between 30% and 50% cases


Abnormality of the dentition Cutaneous photosensitivity Neoplasm of the skin Pain Palmoplantar keratoderma Melanoma Hyperhidrosis Papule Nail dystrophy Carious teeth Seizures Telangiectasia Osteolysis Diarrhea Poikiloderma Sparse hair Hearing impairment Sensorineural hearing impairment Anemia Delayed skeletal maturation Inflammatory abnormality of the skin Esophagitis Skin rash Conjunctivitis Abnormal blistering of the skin Keratitis Thickened skin Short stature Ichthyosis Hypopigmented skin patches Scarring

Rare Symptoms - Less than 30% cases


Increased urinary cortisol level Neuroendocrine neoplasm Pituitary growth hormone cell adenoma Pituitary corticotropic cell adenoma Angiofibromas Fasting hyperinsulinemia Zollinger-Ellison syndrome Thyroid adenoma Pituitary prolactin cell adenoma Extrahepatic cholestasis Subcutaneous lipoma Insulinoma Thymoma Adrenocortical adenoma Carcinoid tumor Peptic ulcer Primary hyperparathyroidism Parathyroid adenoma Elevated circulating parathyroid hormone level Neoplasm of the endocrine system Abnormality of the endocrine system Hyperinsulinemic hypoglycemia Pituitary adenoma Pituitary null cell adenoma Hypogonadism Increased glucagon level Corneal erosion Photophobia Abnormality of the tongue Amniotic constriction ring Oral leukoplakia Reduced tendon reflexes Opacification of the corneal stroma Skin ulcer Nail dysplasia Pruritus Corneal opacity Macule Flexion contracture Alopecia of scalp Confetti-like hypopigmented macules Edema Eczema Hypopigmentation of the skin Abnormality of skin pigmentation Increased circulating cortisol level Osteoporosis Visual impairment Cataract Growth delay Dry skin Dermal atrophy Ectropion Abnormality of pancreas physiology Episodic abdominal pain Parathyroid hyperplasia Growth hormone excess Vomiting Hypertrichosis Thin skin Generalized hirsutism Skin vesicle Fragile skin Atypical scarring of skin Hypotrichosis Recurrent skin infections Palmoplantar hyperkeratosis Scaling skin Gingivitis Periodontitis Premature loss of primary teeth Plantar hyperkeratosis Abnormality of the fingernails Cryptorchidism Hyperparathyroidism Hypercalcemia Keratoconjunctivitis sicca Blepharitis Eczematoid dermatitis Overbite Telangiectasia of the skin Cellulitis Freckling Spotty hypopigmentation Hypermelanotic macule Melanocytic nevus Severe hearing impairment Abnormal eyelash morphology Hemiplegia/hemiparesis Pterygium Dystrophic toenail Intellectual disability, progressive Furrowed tongue Aminoaciduria Hypoplastic fingernail Bone marrow hypocellularity Dystrophic fingernails Corneal neovascularization Abnormal vertebral morphology Recurrent corneal erosions Choreoathetosis Aplasia/Hypoplasia of the eyebrow Hypoplastic toenails Abnormality of the anus Aganglionic megacolon Blindness Visual loss Cerebellar hypoplasia Pes cavus Neoplasm of the eye Arthritis Severe global developmental delay Delayed eruption of teeth Progressive visual loss Defective DNA repair after ultraviolet radiation damage Fine hair Ankyloblepharon Hypohidrosis Abnormality of extrapyramidal motor function Sparse and thin eyebrow Elbow flexion contracture Papilloma Knee flexion contracture Conjunctival telangiectasia Sparse eyelashes Entropion Urticaria Congenital sensorineural hearing impairment Absent eyebrow Urethral stricture Craniofacial hyperostosis Squamous cell carcinoma of the skin Acral blistering Phimosis Spasticity Cutaneous finger syndactyly Overjet Gingival bleeding Turricephaly Fatigue Optic atrophy Abnormality of the skull Diffuse skin atrophy Esophageal stricture Fever Peripheral neuropathy Cognitive impairment Abnormal toenail morphology Symblepharon Strabismus Failure to thrive Ataxia Short 4th metacarpal Scoliosis Ridged nail Cheilitis Microcephaly Neoplasm of the urethra Anal fissure Short 5th metacarpal Telangiectases in sun-exposed and nonexposed skin Aplasia/Hypoplasia of the skin Colitis Ankyloglossia Trichiasis Decreased testicular size Corneal scarring Recurrent bacterial skin infections Developmental regression Mental deterioration Generalized hyperkeratosis Corneal ulceration Laryngeal stenosis Moderate hearing impairment Spotty hyperpigmentation Severe photosensitivity EEG abnormality Abnormality of corneal stroma Hyporeflexia Dysphagia Syndactyly Camptodactyly of finger Finger syndactyly Abnormality of the ribs Abnormality of dental enamel Arthralgia Abnormality of the hand Cerebral cortical atrophy Inflammation of the large intestine Milia Atrophic scars Keratoconjunctivitis Striae distensae Skin fissure Steatorrhea Severe periodontitis Chronic furunculosis Halitosis Atrophy of alveolar ridges Abdominal pain Weight loss Hypoglycemia Nausea Cafe-au-lait spot Elevated alkaline phosphatase Pyloric stenosis Intestinal obstruction Glucose intolerance Abnormality of the thyroid gland Recurrent cutaneous abscess formation Multiple lipomas Lipoma Hyperaldosteronism Prolactin excess Neoplasm of the pancreas Peritonitis Pheochromocytoma Bone cyst Schwannoma Adenoma sebaceum Epigastric pain Adrenocortical carcinoma Neurofibrosarcoma Choroid plexus calcification Cigarette-paper scars Anterior pituitary dysgenesis Congenital hypoplastic anemia Abnormality of the liver Cirrhosis Hemolytic anemia Hepatic steatosis Sudden cardiac death Hepatitis Hyperpigmentation of the skin Cerebral palsy Scleroderma Hepatocellular carcinoma Onycholysis Anemia of inadequate production Alcoholism Facial hypertrichosis Liver abscess Viral hepatitis Porphyrinuria Hyperpigmentation in sun-exposed areas Recurrent respiratory infections Arachnodactyly Cerebral calcification Abnormality of the nail Reduced number of teeth Sparse body hair Premature loss of teeth Pustule Fragile nails Stomatitis Abnormality of the anterior pituitary Glucagonoma Circumungual hyperkeratosis Pili torti Global developmental delay Severe short stature Joint laxity Hypodontia Ectodermal dysplasia Epidermal acanthosis Cutis laxa Mutism Anhidrosis Curly hair Parakeratosis Neoplasm of the lung Ankylosis Hypergranulosis Lamellar cataract Generalized osteoporosis Subungual hyperkeratosis Trichorrhexis nodosa Alopecia universalis Abnormal cornea morphology Abnormal oral mucosa morphology Abnormality of the gingiva Palmoplantar hyperhidrosis Hidrotic ectodermal dysplasia Autoamputation Foot pain Ainhum Agenesis of premolar Acrokeratosis Acantholysis Prolactinoma Renal angiomyolipoma Pancreatic islet cell adenoma Pancreatic endocrine tumor Hypertension Diabetes mellitus Hypothyroidism Type II diabetes mellitus Abnormality of the urinary system Thyroiditis Hashimoto thyroiditis Thyroid carcinoma Papillary thyroid carcinoma Testicular neoplasm Parathyroid carcinoma Pulmonary carcinoid tumor Concave nasal ridge Cervix cancer Feeding difficulties Frontal bossing Prominent forehead Osteopenia Postnatal growth retardation Leukemia Overgrowth Sparse scalp hair Erythroderma Basal cell carcinoma Severe vision loss Osteosarcoma Flat nasal alae



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