Abnormal blood vessel morphology
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HP_0033353 |
[Any structural anomaly of a blood vessel (artery, arteriole, capillary, venule, or vein).] |
Abnormality of the pulmonary vasculature
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HP_0004930 |
|
Abnormality of the vasculature
|
HP_0002597 |
|
Abnormal lung morphology
|
HP_0002088 |
|
Negative Test Result
|
NCIT_C35681 |
|
Clinical Test Result
|
NCIT_C77140 |
|
Positive Laboratory Test Result
|
NCIT_C35682 |
|
Laboratory Test Result
|
NCIT_C36292 |
|
[X] familial severe combined immunodeficiency
|
MONDO_0031520 |
|
severe combined immunodeficiency
|
MONDO_0015974 |
[Severe combined immunodeficiency (SCID) comprises a group of rare monogenic primary immunodeficiency disorders characterized by a lack of functional peripheral T lymphocytes resulting in early-onset severe respiratory infections and failure to thrive. They are classified according to immunological phenotype into SCID with absence of T cells but presence of B cells (T-B+ SCID) or SCID with absence of both (T-B- SCID). Both of these groups include several forms, with or without natural killer (NK) cells.] |
leg dermatosis
|
MONDO_0006569 |
[A nonspecific term used to denote any cutaneous lesion or group of lesions, or eruptions of any type on the leg. (From Stedman, 25th ed)] |
kernicterus due to isoimmunization
|
MONDO_0006567 |
[Encephalopathy in infants due to high levels of unconjugated bilirubin that are a result of Rh incompatibility between the mother and the fetus.] |
[X] bilirubin encephalopathy
|
MONDO_0018477 |
|
[X] neonatal anemia
|
MONDO_0001240 |
[The mildest form of erythroblastosis fetalis in which anemia is the chief manifestation.] |
obsolete Kimura disease
|
MONDO_0006568 |
|
juvenile dermatitis herpetiformis
|
MONDO_0006565 |
[Dermatitis herpetiformis in children] |
dermatitis herpetiformis
|
MONDO_0015614 |
[Dermatitis herpetiformis (DH) is a chronic autoimmune subepidermal bullous disease characterized by grouped pruritic lesions such as papules, urticarial plaques, erythema, and herpetiform vesiculae, with a predominantly symmetrical distribution on extensor surfaces of the elbows (90%), knees (30%), shoulders, buttocks, sacral region, and face of children and adults. Erosions, excoriations and hyperpigmentation usually follow. DH may also appear as a consequence of gluten intolerance.] |
[X] keratinization disease
|
MONDO_0045011 |
|
[X] inverted follicular keratosis
|
MONDO_0006563 |
[Seborrheic keratosis that arises from follicular structures in the skin. It presents as a solitary nodule in the skin and is characterized by the presence of prominent squamous eddies.] |
seborrheic keratosis
|
MONDO_0008420 |
[A common benign skin neoplasm usually affecting older individuals. The lesions usually are multiple and arise in the face, chest, and shoulders. They appear as black or brown, slightly elevated skin lesions.] |