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Items: 5

  • The following terms were not found in MedGen: K1op.opphioptcapital, Cyrillic.
1.

BLOOD GROUP--En

MedGen UID:
354697
Concept ID:
C1862238
Intellectual Product
2.

Erythrokeratoderma en cocardes

A rare, genetic, epidermal disorder characterized by intermittent (remitting and recurring), annular, polycyclic, target-like (or 'en cocardes') plaques with concentric rings of scaling erythema occurring on the extremities, flexural areas, and trunk. Concurrent erythrokeratoderma variabilis-like scaly plaques are commonly found in other parts of the body. [from ORDO]

MedGen UID:
1845700
Concept ID:
C5848050
Disease or Syndrome
3.

Ring chromosome 21

Ring chromosome 21 syndrome is an autosomal anomaly characterized by variable clinical features, most commonly including growth retardation, developmental delay, intellectual disability, epilepsy, microcephaly, short stature, dysmorphic features, hypogammaglobulinemia, thrombocytopenia and unspecific skeletal anomalies (hemivertebrae, clinodactyly, syndactyly). In rare cases, it has been described in phenotypically normal individuals. [from ORDO]

MedGen UID:
419409
Concept ID:
C2931422
Cell or Molecular Dysfunction
4.

Malignant atrophic papulosis

Malignant atrophic papulosis (MAP) is a rare, chronic, thrombo-obliterative vasculopathy characterized by papular skin lesions with central porcelain-white atrophy and a surrounding teleangiectatic rim. Systemic lesions may affect the gastrointestinal tract and the central nervous system (CNS) and are potentially lethal. [from ORDO]

MedGen UID:
113138
Concept ID:
C0221011
Disease or Syndrome
5.

Erythema nodosum

An erythematous eruption commonly associated with drug reactions or infection and characterized by inflammatory nodules that are usually tender, multiple, and bilateral. [from HPO]

MedGen UID:
41858
Concept ID:
C0014743
Disease or Syndrome
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