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Cranium bifidum occultum
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HP_0004423 |
[Cranium bifidum occultum, also known as Catlin mark, is a congenital midline skull defect presenting as an enlarged posterior fontanelle in the upper posterior angle of the parietal bone close to the intersection of the sagittal and lambdoid sutures. Cranium bifidum occultum occurs due to a defect in intramembranous ossification, a process through which skull bones (frontal, parietal, squamous temporal and occipital bones superior to the mendosal suture) ossify under a vascularized membrane toward the midline to cover the brain. Unlike cranium bifidum cysticum, cranium bifidum occultum does not have herniation of intracranial contents. As the skull grows, the midline cranium bifidum occultum defect is separated into bilateral enlarged parietal foramina (EPF) by a midline osseous bridge.] |
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Kit-negative, Ly-76 high basophilic erythroblast
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CL_0002014 |
[A basophilic erythroblast that is Lyg 76-high and is Kit-negative.] |
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Arterial thrombosis
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HP_0004420 |
[The formation of a blood clot inside an artery.] |
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hyaluronate
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CHEBI_132153 |
[A carbohydrate acid derivative anion obtained by deprotonation of the carboxy groups of hyaluronic acid; major species at pH 7.3.] |
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pre-conventional dendritic cell
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CL_0002010 |
[A lin-negative, MHC-II-negative, CD11c-positive, FLT3-positive cell with intermediate expression of SIRP-alpha.] |
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Carotid paraganglioma
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HP_0100635 |
[A paraganglioma (a neuroendocrine neoplasm) originating in a carotid artery.] |
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Pulmonary paraglioma
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HP_0100636 |
[A rare paranglioma of the lung, tumors that arise from extra-adrenal chromaffin cells.] |
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obsolete Neoplasia of the nose
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HP_0100637 |
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Ly-76 high reticulocyte
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CL_0002019 |
[A reticulocyte that is Ly76-high and is Kit-negative.] |
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CD9-positive, CD41-positive megakaryocyte cell
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CL_0002027 |
[A megakaryocyte cell with is CD9-positive and CD41-positive.] |
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basophil mast progenitor cell
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CL_0002028 |
[A cell type that can give rise to basophil and mast cells. This cell is CD34-positive, CD117-positive, CD125-positive, FceRIa-negative, and T1/ST2-negative, and expresses Gata-1, Gata-2, C/EBPa] |
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Hyperostosis frontalis interna
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HP_0004438 |
[Bony overgrowth of the internal (endosteal) surface of the frontal bone.] |
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Fc-epsilon RIalpha-low mast cell progenitor
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CL_0002029 |
[A lineage-negative, Kit-positive, CD45-positive mast cell progenitor that is Fc-epsilon RIalpha-low.] |
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Secretory IgA deficiency
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HP_0004433 |
[Deficiency of secretory IgA (polymers of 2-4 IgA monomers are linked by two additional chains) and is the primary antibody response at the mucosal level, where it forms immune complexes with pathogens and allergens.] |
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bracket
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PATO_0002142 |
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Ly-76 high positive erythrocyte
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CL_0002022 |
[An enucleate erythrocyte that is Lyg-76-high.] |
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Agammaglobulinemia
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HP_0004432 |
[A lasting absence of total IgG and total IgA and total IgM in the blood circulation, whereby at most trace quantities can be measured.] |
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sloped downward
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PATO_0002143 |
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Kit-positive megakaryocyte progenitor cell
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CL_0002024 |
[A megakaryocyte progenitor cell that is Kit-positive, CD41-positive, CD9-positive, Sca-1-negative, IL7ralpha-negative, CD150-negative, and Fcgamma receptor II/III-low.] |
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Decreased circulating complement C8 concentration
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HP_0004434 |
[Concentration of the complement component C8 in the blood circulation below the lower limit of normal.] |