Terminology Service < Semantic Lookup Platform

All terms in HP

Label	Id	Description
Aplasia of the uterus	HP_0000151	[Aplasia of the uterus.]
Aplasia/hypoplasia of the uterus	HP_0008684	[Absence or developmental hypoplasia of the uterus.]
Abnormality of head or neck	HP_0000152	[An abnormality of head and neck.]
Phenotypic abnormality	HP_0000118	[A phenotypic abnormality.]
N-acyl-L-amino acid	CHEBI_21644	[Any N-acylamino acid having L-configuration.]
N-acyl-D-amino acid	CHEBI_15778	[Any N-acyl-amino acid in which the amino acid moiety has D configuration.]
Abnormal granulocytopoietic cell morphology	HP_0012135	[An anomaly of cells involved in the formation of a granulocytes, that is, of the granulocytopoietic cell.]
Dysplastic erythropoesis	HP_0012134
Abnormal erythrocyte morphology	HP_0001877	[Any structural abnormality of erythrocytes (red-blood cells).]
Erythroid hypoplasia	HP_0012133	[Decreased count of erythroid precursor cells, that is, erythroid lineage cells in the bone marrow.]
Abnormal number of erythroid precursors	HP_0012131	[A deviation from the normal count of erythroid precursor cells, that is, erythroid lineage cells in the bone marrow.]
Erythroid hyperplasia	HP_0012132	[Increased count of erythroid precursor cells, that is, erythroid lineage cells in the bone marrow.]
Granulocytic hypoplasia	HP_0012139	[Decreased number of granulocyte precursors in the bone marrow.]
Abnormal number of granulocyte precursors	HP_0012137
Granulocytic hyperplasia	HP_0012138
Dysplastic granulopoesis	HP_0012136
consumption behavior	NBO_0001845
behavior process	NBO_0000313
Abnormal erythroid lineage cell morphology	HP_0012130	[An anomaly of erythroid lineage cells, that is, of the erythropoietic cells in the lineage leading to and including erythrocytes.]
Abnormal myeloid cell morphology	HP_0020047	[Any structural anomaly of a cell of the monocyte, granulocyte, mast cell, megakaryocyte, or erythroid lineage.]