All terms in HP

Label Id Description
cell adhesion molecule CEACAM8 PR_000001332 [A protein that is a translation product of the human CEACAM8 gene or a 1:1 ortholog thereof.]
Bridged palmar crease HP_0011310 [A crease that connects the proximal and distal transverse palmar creases.]
Narrow nail HP_0011313 [Decreased width of nail.]
Sydney crease HP_0011311 [Extension of the proximal transverse crease (five finger crease) to the ulnar edge of the palm.]
Fused nails HP_0011312 [A nail plate that has a longitudinal separation with partially separated nails, each with a separate lateral radius of curvature.]
Neonatal hypoglycemia HP_0001998
Anterior plagiocephaly HP_0011326 [Asymmetry of the anterior part of the skull.]
Posterior plagiocephaly HP_0011327 [Asymmetry of the posterior part of the skull.]
Unilambdoid synostosis HP_0011320 [Premature synostosis of only one lambdoid suture.]
Left unilambdoid synostosis HP_0011321 [Premature synostosis of only the left lambdoid suture.]
Multiple suture craniosynostosis HP_0011324 [Craniosynostosis involving at least 2 cranial sutures, where the exact pattern of sutures fused has not been precisely specified.]
Pansynostosis HP_0011325 [Craniosynostosis of all calvarial sutures.]
Right unilambdoid synostosis HP_0011322 [Premature synostosis of only the right lambdoid suture.]
Cleft of chin HP_0011323 [Incomplete fusion of the chin, resulting from a developmental defect and manifesting as a midline cleft or fissure of the chin.]
mesenchymal cell proliferation involved in lung development GO_0060916 [The multiplication or reproduction of cells, resulting in the expansion of a mesenchymal cell population that contributes to the progression of the lung over time. A mesenchymal cell is a cell that normally gives rise to other cells that are organized as three-dimensional masses, rather than sheets.]
Hemifacial atrophy HP_0011331 [Unilateral atrophy of facial tissues, including muscles, bones and skin.]
Hemifacial hypoplasia HP_0011332 [Unilateral underdevelopment of the facial tissues, including muscles and bones.]
Metopic synostosis HP_0011330 [Premature fusion of the metopic suture.]
Frontal hirsutism HP_0011335 [Excessive amount of hair growth on forehead.]
Bitemporal forceps marks HP_0011336 [Bilateral temporal scarlike defects, which are said to resemble forceps marks.]