Inbound Relationships |
Type |
Active |
Source |
Characteristic |
Refinability |
Group |
Hypoparathyroidism due to hemochromatosis (disorder) |
Has definitional manifestation |
False |
Decreased hormone secretion |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Transient neonatal hypoparathyroidism due to maternal hyperparathyroidism (disorder) |
Has definitional manifestation |
False |
Decreased hormone secretion |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Secondary hypoparathyroidism (disorder) |
Has definitional manifestation |
False |
Decreased hormone secretion |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypoparathyroidism due to granulomatous disease (disorder) |
Has definitional manifestation |
False |
Decreased hormone secretion |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare multiple congenital anomalies/dysmorphic syndrome characterized by the association of congenital hypoparathyroidism, nephropathy, congenital lymphedema, mitral valve prolapse and brachytelephalangy. Additional features include mild facial dysmorphism, hypertrichosis, and nail abnormalities. There have been no further descriptions in the literature since 1993. |
Has definitional manifestation |
False |
Decreased hormone secretion |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypoparathyroidism following procedure (disorder) |
Has definitional manifestation |
False |
Decreased hormone secretion |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare heterogeneous group of metabolic disorders characterized by abnormal calcium metabolism causing hypocalcemia due to insufficient serum levels of bioactive parathormone (PTH), without other endocrine disorders or developmental defects. |
Has definitional manifestation |
False |
Decreased hormone secretion |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypoparathyroidism, deafness, renal disease syndrome (disorder) |
Has definitional manifestation |
False |
Decreased hormone secretion |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare heterogeneous group of metabolic disorders characterized by abnormal calcium metabolism causing hypocalcemia due to insufficient serum levels of bioactive parathormone (PTH), without other endocrine disorders or developmental defects. |
Is a |
False |
Decreased hormone secretion |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
A rare genetic disease characterized by sclerosing dysplasia affecting the diaphyseal and metaphyseal regions of the long bones, as well as the skull and metacarpals, in association with skin changes like those seen in ichthyosis vulgaris and premature ovarian failure with bilateral hypoplasia of the ovaries. Patients present in adulthood, primarily with swelling of the extremities and occasional mild pain in the legs. |
Is a |
False |
Decreased hormone secretion |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypoparathyroidism, deafness, renal disease syndrome (disorder) |
Is a |
False |
Decreased hormone secretion |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Hypoparathyroidism |
Is a |
True |
Decreased hormone secretion |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Ovarian failure |
Is a |
True |
Decreased hormone secretion |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|
Decreased placental secretion of chorionic gonadotropin |
Is a |
True |
Decreased hormone secretion |
Inferred relationship |
Existential restriction modifier (core metadata concept) |
|