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1.

Fanconi anemia complementation group U

Fanconi anemia (FA) is characterized by physical abnormalities, bone marrow failure, and increased risk for malignancy. Physical abnormalities, present in approximately 75% of affected individuals, include one or more of the following: short stature, abnormal skin pigmentation, skeletal malformations of the upper and/or lower limbs, microcephaly, and ophthalmic and genitourinary tract anomalies. Progressive bone marrow failure with pancytopenia typically presents in the first decade, often initially with thrombocytopenia or leukopenia. The incidence of acute myeloid leukemia is 13% by age 50 years. Solid tumors – particularly of the head and neck, skin, and genitourinary tract – are more common in individuals with FA. [from GeneReviews]

MedGen UID:
934618
Concept ID:
C4310651
Disease or Syndrome
2.

Symphalangism, distal, with microdontia, dental pulp stones, and narrowed zygomatic arch

MedGen UID:
376067
Concept ID:
C1847185
Disease or Syndrome
3.

Absent scaphoid

Congenital absence of the scaphoid.. [from HPO]

MedGen UID:
337748
Concept ID:
C1847189
Finding
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