Anemia, and Psoriasiform dermatitis

Diseases related with Anemia and Psoriasiform dermatitis

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


Top matches:

Medium match MAJEED SYNDROME; MJDS


MAJEED SYNDROME; MJDS Is also known as chronic recurrent multifocal osteomyelitis, congenital dyserythropoietic anemia, and neutrophilic dermatosis

Related symptoms:

  • Growth delay
  • Anemia
  • Flexion contracture
  • Fever
  • Delayed skeletal maturation


SOURCES: OMIM MENDELIAN

More info about MAJEED SYNDROME; MJDS

Medium match IDIOPATHIC CD4 LYMPHOCYTOPENIA


Idiopathic CD4 lymphocytopenia is a rare primary immunodeficiency disorder characterized by persistent CD4 T-cell lymphopenia (less than 300 cells/µL on multiple occasions) not associated with any other underlying primary or secondary immune deficiency. Patients typically present opportunistic infections (with cryptococcal, mycobacterial, candidal, varicella zoster virus infections and progressive multifocal leukoencephalopathy being the most prevalent), malignancies (mainly lymphoproliferative disorders), or autoimmune disorders. Some individuals are asymptomatic and incidentally diagnosed.

IDIOPATHIC CD4 LYMPHOCYTOPENIA Is also known as icl|idiopathic cd4 lymphopenia

Related symptoms:

  • Neoplasm
  • Anemia
  • Immunodeficiency
  • Pneumonia
  • Carcinoma


SOURCES: OMIM ORPHANET MENDELIAN

More info about IDIOPATHIC CD4 LYMPHOCYTOPENIA

Medium match AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME DUE TO CTLA4 HAPLOINSUFFIENCY


Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency is a rare, primary immunodeficiency characterized by variable combination of enteropathy, hypogammaglobulinemia, recurrent respiratory infections, granulomatous lymphocytic interstitial lung disease, lymphocytic infiltration of non-lymphoid organs (intestine, lung, brain, bone marrow, kidney), autoimmune thrombocytopenia or neutropenia, autoimmune hemolytic anemia and lymphadenopathy.

AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME DUE TO CTLA4 HAPLOINSUFFIENCY Is also known as alps due to ctla4 haploinsuffiency|chai|ctla4 haploinsufficiency with autoimmune infiltration|ctla-4 haploinsufficiency with autoimmune infiltration disease

Related symptoms:

  • Hepatomegaly
  • Diarrhea
  • Splenomegaly
  • Immunodeficiency
  • Recurrent infections


SOURCES: OMIM ORPHANET MENDELIAN

More info about AUTOIMMUNE LYMPHOPROLIFERATIVE SYNDROME DUE TO CTLA4 HAPLOINSUFFIENCY

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Other less relevant matches:

Medium match IMMUNODEFICIENCY DUE TO CD25 DEFICIENCY


Immunodeficiency due to CD25 deficiency is a rare, genetic, primary immunodeficiency due to a defect in adaptive immunity disorder characterized by severe immunodeficiency, presenting with profound susceptibility to viral, fungal and bacterial infections due to impaired CD25-mediated T-regulatory cell function, in association with severe autoimmune disease, such as alopecia universalis, erythrodermia, and autoimmune thyroiditis and enteropathy.

IMMUNODEFICIENCY DUE TO CD25 DEFICIENCY Is also known as cd25 deficiency|interleukin 2 receptor, alpha, deficiency of|interleukin-2 receptor alpha chain deficiency|il2ra deficiency

Related symptoms:

  • Anemia
  • Hepatomegaly
  • Respiratory insufficiency
  • Diarrhea
  • Splenomegaly


SOURCES: MESH ORPHANET OMIM MENDELIAN

More info about IMMUNODEFICIENCY DUE TO CD25 DEFICIENCY

Medium match COMBINED IMMUNODEFICIENCY-ENTEROPATHY SPECTRUM


COMBINED IMMUNODEFICIENCY-ENTEROPATHY SPECTRUM Is also known as cid-mia/early-onset ibd

Related symptoms:

  • Intrauterine growth retardation
  • Ventricular septal defect
  • Immunodeficiency
  • Polyhydramnios
  • Sparse hair


SOURCES: ORPHANET MENDELIAN

More info about COMBINED IMMUNODEFICIENCY-ENTEROPATHY SPECTRUM

Medium match TAKAYASU ARTERITIS


Takayasu arteritis (TAK) is a rare inflammatory large-vessel vasculitis primarily affecting the aorta and its major branches, but also other large vessels, causing stenosis, occlusion, or aneurysm.

TAKAYASU ARTERITIS Is also known as young female arteritis|aortic arch syndrome|pulseless disease

Related symptoms:

  • Seizures
  • Muscle weakness
  • Anemia
  • Hypertension
  • Fever


SOURCES: ORPHANET OMIM MENDELIAN

More info about TAKAYASU ARTERITIS

Medium match MULTIPLE INTESTINAL ATRESIA


Multiple intestinal atresia is a rare form of intestinal atresia characterized by the presence of numerous atresic segments in the small bowel (duodenum) or large bowel and leading to symptoms of intestinal obstruction: vomiting, abdominal bloating and inability to pass meconium in newborns.

MULTIPLE INTESTINAL ATRESIA Is also known as intestinal atresia, multiple|minat|intestinal atresia, multiple and/or inflammatory bowel disease with or without immunodeficiency|fipa|familial intestinal polyatresia syndrome

Related symptoms:

  • Growth delay
  • Anemia
  • Intrauterine growth retardation
  • Abnormality of the skeletal system
  • Ventricular septal defect


SOURCES: ORPHANET OMIM MESH MENDELIAN

More info about MULTIPLE INTESTINAL ATRESIA

Medium match PEUTZ-JEGHERS SYNDROME; PJS


Peutz-Jeghers syndrome is an autosomal dominant disorder characterized by melanocytic macules of the lips, buccal mucosa, and digits; multiple gastrointestinal hamartomatous polyps; and an increased risk of various neoplasms.

PEUTZ-JEGHERS SYNDROME; PJS Is also known as polyps-and-spots syndrome|polyposis, hamartomatous intestinal

Related symptoms:

  • Neoplasm
  • Hypertension
  • Edema
  • Diarrhea
  • Headache


SOURCES: OMIM MENDELIAN

More info about PEUTZ-JEGHERS SYNDROME; PJS

Medium match SINGLETON-MERTEN DYSPLASIA


Singleton-Merten dysplasia is characterized by dental dysplasia, progressive calcification of the thoracic aorta with stenosis, osteoporosis and expansion of the marrow cavities in hand bones. Additional features included generalized muscle weakness and atrophy, and chronic psoriasiform skin eruptions. It has been reported in four unrelated patients (male and female) and in a family with multiple affected members (male).

SINGLETON-MERTEN DYSPLASIA Is also known as singleton-merten syndrome

Related symptoms:

  • Global developmental delay
  • Short stature
  • Generalized hypotonia
  • Growth delay
  • Muscle weakness


SOURCES: OMIM ORPHANET MENDELIAN

More info about SINGLETON-MERTEN DYSPLASIA

Medium match PROLIDASE DEFICIENCY


Prolidase deficiency is an inherited disorder of peptide metabolism characterized by severe skin lesions, recurrent infections (involving mainly the skin and respiratory system), dysmorphic facial features, variable cognitive impairment, and splenomegaly.

PROLIDASE DEFICIENCY Is also known as hyperimidodipeptiduria

Related symptoms:

  • Intellectual disability
  • Global developmental delay
  • Hearing impairment
  • Hypertelorism
  • Micrognathia


SOURCES: ORPHANET MESH OMIM MENDELIAN

More info about PROLIDASE DEFICIENCY

Top 5 symptoms//phenotypes associated to Anemia and Psoriasiform dermatitis

Symptoms // Phenotype % cases
Diarrhea Uncommon - Between 30% and 50% cases
Autoimmune hemolytic anemia Uncommon - Between 30% and 50% cases
Immunodeficiency Uncommon - Between 30% and 50% cases
Recurrent infections Uncommon - Between 30% and 50% cases
Recurrent respiratory infections Uncommon - Between 30% and 50% cases
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Other less frequent symptoms

Patients with Anemia and Psoriasiform dermatitis. may also develop some of the following symptoms:

Uncommon Symptoms - Between 30% and 50% cases


Inflammatory abnormality of the skin Bloody diarrhea Hepatitis Hepatomegaly Growth delay Splenomegaly Abdominal distention Abnormal lung morphology Abnormal intestine morphology Thyroiditis Hemolytic anemia Lymphopenia Type I diabetes mellitus Hepatosplenomegaly Hypertension

Rare Symptoms - Less than 30% cases


Polyhydramnios Genu valgum Carious teeth Nail dystrophy Autoimmunity Sparse hair Ventricular septal defect Skin ulcer Ptosis Abnormal facial shape Intrauterine growth retardation Chronic lung disease Global developmental delay Iron deficiency anemia Increased antibody level in blood Cutaneous photosensitivity Congenital cystic adenomatoid malformation of the lung Peritoneal abscess Intestinal atresia Gastrointestinal atresia Jejunoileal ulceration Abnormality of the ductus choledochus Rectal abscess Muscle weakness Ectopic calcification Alopecia Intestinal malrotation Severe combined immunodeficiency Alopecia of scalp Hashimoto thyroiditis Absent eyebrow Thickened skin Omphalocele Dilatation Hyperhidrosis Hypoplasia of the thymus Skin rash Osteomyelitis Eczema Decreased antibody level in blood Lymphadenopathy Fever Respiratory tract infection Arthritis Thrombocytopenia Arthralgia Bronchiolitis Neoplasm Pneumonia Carcinoma Generalized muscle weakness Hypoplasia of the maxilla Smooth philtrum Facial hirsutism Cardiomegaly Waddling gait Convex nasal ridge Decreased body weight Subvalvular aortic stenosis Premature loss of permanent teeth Mitral valve calcification Hip subluxation Aortic valve calcification Shallow acetabular fossae Muscle fiber atrophy Onycholysis Coxa valga Osteolytic defects of the phalanges of the hand High anterior hairline Periodontitis Heart block Epiphora Scaling skin Osteolysis Aortic valve stenosis Thin upper lip vermilion Hip dislocation Muscular hypotonia Intestinal polyp Intussusception Clear cell renal cell carcinoma Gastrointestinal carcinoma Uterine neoplasm Thyroid nodule Congenital shortened small intestine Endolymphatic sac tumor Precocious puberty with Sertoli cell tumor Diffuse telangiectasia Short stature Generalized hypotonia Crusting erythematous dermatitis Broad forehead Myopia Skeletal muscle atrophy Talipes equinovarus Congestive heart failure Abnormality of the dentition Visual loss Arrhythmia Pes cavus Osteoporosis Glaucoma Osteopenia Dentinogenesis imperfecta limited to primary teeth Joint laxity Unerupted tooth Expanded metacarpals with widened medullary cavities Tendon rupture Proptosis Reduced bone mineral density Abnormality of the fingernails Generalized hirsutism Recurrent pneumonia Bilateral single transverse palmar creases Low anterior hairline Lymphedema Malar flattening Abnormality of metabolism/homeostasis Obesity Prominent forehead Hyperkeratosis High forehead Thrombophlebitis Abnormality of retinal pigmentation Elevated hepatic transaminase Erythema Papule Pruritus Thin skin Arachnodactyly Depressed nasal ridge Dry skin Low posterior hairline Hirsutism Palmoplantar keratoderma Asthma Systemic lupus erythematosus Petechiae Hypoplasia of the tooth germ Visual impairment Aortic arch calcification Expanded metatarsals with widened medullary cavities Hypoplastic distal radial epiphyses Dehydration Poliosis Expanded phalanges with widened medullary cavities Intellectual disability Hearing impairment Hypertelorism Micrognathia High palate Delayed speech and language development Depressed nasal bridge Elevated erythrocyte sedimentation rate Downslanted palpebral fissures Intellectual disability, severe Abnormality of the middle ear White forelock Vomiting Concave nasal ridge Hypoplasia of the zygomatic bone Intellectual disability, mild Short nose Prolonged neonatal jaundice Abnormality of the immune system Aplasia/Hypoplasia of the skin Abnormality of the hip bone Testicular neoplasm Abdominal pain Hematemesis Recurrent abscess formation IgA deficiency Atopic dermatitis Gingivitis Antinuclear antibody positivity Esophagitis Recurrent viral infections Villous atrophy Immune dysregulation Decrease in T cell count Recurrent fungal infections Granulocytopenia Chronic hemolytic anemia Seizures Chronic diarrhea Fatigue Weight loss Myalgia Hypertrophic cardiomyopathy Retinopathy Neurological speech impairment Chest pain Migraine Pulmonary arterial hypertension Myocardial infarction Subcutaneous nodule Anorexia Vasculitis Recurrent bacterial infections Hypothyroidism Abnormal heart valve morphology Sinusitis Flexion contracture Delayed skeletal maturation Bone pain Microcytic anemia Episodic fever Anemia of inadequate production Decreased mean corpuscular volume Congenital hypoplastic anemia Low-grade fever Chronic recurrent multifocal osteomyelitis Lymphoma Otitis media Recurrent otitis media Squamous cell carcinoma Diabetes mellitus Recurrent sinusitis Hodgkin lymphoma Papilloma Bronchiolitis obliterans Opportunistic infection Bronchiolitis obliterans organizing pneumonia Recurrent upper respiratory tract infections Interstitial pulmonary abnormality Autoimmune thrombocytopenia Verrucae Impaired T cell function Decreased proportion of CD4-positive T cells Respiratory insufficiency Aortic regurgitation Hemoptysis Intestinal bleeding Abnormality of the ureter Accelerated skeletal maturation Hemangioma Breast carcinoma Growth abnormality Polycystic kidney dysplasia Melanocytic nevus Clubbing Intestinal obstruction Hypermelanotic macule Macule Hamartoma Ovarian neoplasm Renal cell carcinoma Nevus Vitiligo Abnormality of the mouth Neoplasm of the pancreas Clubbing of fingers Multiple myeloma Ovarian cyst Intestinal polyposis Pancreatic cysts Biliary tract abnormality Rectal prolapse Nasal polyposis Neoplasm of the breast Hamartomatous polyposis Gynecomastia Abnormality of the kidney Gangrene Abnormality of the skeletal system Cerebral ischemia Reduced consciousness/confusion Abnormal aortic valve morphology Inflammatory abnormality of the eye Abnormal pattern of respiration Arterial stenosis Ascending tubular aorta aneurysm Abnormal endocardium morphology Amaurosis fugax Gastrointestinal infarctions Arteritis Hypertensive crisis Increased inflammatory response Scarring Headache Small for gestational age Anal atresia Sepsis Inflammation of the large intestine Combined immunodeficiency Abnormality of abdomen morphology Hematochezia Duodenal atresia Duodenal stenosis Microcolon Jejunal atresia Decreased proportion of CD8-positive T cells Edema Recurrent cystitis



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