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Items: 6

1.

Amyloidosis cutis dyschromia

A rare primary cutaneous amyloidosis characterized by macular or reticulate hyperpigmentation with symmetrically distributed guttate hypo and hyperpigmented lesions which progress gradually over the years to involve almost the entire body (with relative sparing of the face, hands, feet and neck). Patients are usually asymptomatic, however mild pruritus may be associated. Amyloid deposition in the papillary dermis is observed on skin biopsy. Systemic amyloidosis is not present and association with generalized morphea, atypical Parkinsonism, spasticity, motor weakness or colon carcinoma is rare. [from SNOMEDCT_US]

MedGen UID:
1641859
Concept ID:
C4554601
Disease or Syndrome
2.

Anorectal malformation

MedGen UID:
988249
Concept ID:
CN305294
Disease or Syndrome
3.

Cerebral cavernous malformation

Cerebral cavernous malformations (CCMs) are vascular malformations in the brain and spinal cord comprising closely clustered, enlarged capillary channels (caverns) with a single layer of endothelium without mature vessel wall elements or normal intervening brain parenchyma. The diameter of CCMs ranges from a few millimeters to several centimeters. CCMs increase or decrease in size and increase in number over time. Hundreds of lesions may be identified, depending on the person's age and the quality and type of brain imaging used. Although CCMs have been reported in infants and children, the majority become evident between the second and fifth decades with findings such as seizures, focal neurologic deficits, nonspecific headaches, and cerebral hemorrhage. Up to 50% of individuals with FCCM remain symptom free throughout their lives. Cutaneous vascular lesions are found in 9% of those with familial cerebral cavernous malformations (FCCM; see Diagnosis/testing) and retinal vascular lesions in almost 5%. [from GeneReviews]

MedGen UID:
418825
Concept ID:
C2919945
Congenital Abnormality
4.

Zonular cataract

Zonular cataracts are defined to be cataracts that affect specific regions of the lens. [from HPO]

MedGen UID:
350517
Concept ID:
C1861821
Disease or Syndrome
5.

Avellino corneal dystrophy

Type II granular corneal dystrophy (GCDII) is a rare form of stromal corneal dystrophy (see this term) characterized by irregular-shaped well-demarcated granular deposits in the superficial central corneal stroma, and progressive visual impairment. [from ORDO]

MedGen UID:
220900
Concept ID:
C1275685
Disease or Syndrome
6.

Short humerus

Underdevelopment of the humerus. [from HPO]

MedGen UID:
316907
Concept ID:
C1832117
Congenital Abnormality; Finding
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