not genetically inherited
http://www.orpha.net/ORDO/Orphanet_409941
clinical entity without genetic inheritance.
Term info
Term relations
Related from:
has_inheritance
- Sporadic idiopathic steroid-resistant nephrotic syndrome
- Semilobar holoprosencephaly
- Diffuse cutaneous systemic sclerosis
- Immunotactoid glomerulopathy
- Non-amyloid fibrillary glomerulopathy
- Pauci-immune glomerulonephritis without ANCA
- Pauci-immune glomerulonephritis with ANCA
- Congenital trigeminal anesthesia
- Hepatitis delta
- Sporadic idiopathic steroid-resistant nephrotic syndrome with collapsing glomerulopathy
- Optic pathway glioma
- Pseudohypoparathyroidism
- 49,XXXXY syndrome
- 48,XXXY syndrome
- Cushing disease
- Myeloid sarcoma
- Closed iniencephaly
- Plasmacytoma
- Open iniencephaly
- Spina bifida aperta
- Total spina bifida aperta
- Lymphomatoid granulomatosis
- Paroxysmal non-kinesigenic dyskinesia
- Paroxysmal exertion-induced dyskinesia
- Autosomal dominant dopa-responsive dystonia
- Aggressive NK-cell leukemia
- Cervical spina bifida aperta
- Adult T-cell leukemia/lymphoma
- CD4+/CD56+ hematodermic neoplasm
- Paroxysmal kinesigenic dyskinesia
- Lumbosacral spina bifida aperta
- Thoracolumbosacral spina bifida aperta
- Extranodal nasal NK/T cell lymphoma
- Subcutaneous panniculitis-like T-cell lymphoma
- Cervicothoracic spina bifida aperta
- Choanal atresia, unilateral
- Choanal atresia
- Aggressive systemic mastocytosis
- Mast cell leukemia
- Systemic mastocytosis with an associated clonal hematologic non-mast cell lineage disease
- Indolent systemic mastocytosis
- Refractory anemia with excess blasts
- Juvenile myelomonocytic leukemia
- Primary mediastinal large B-cell lymphoma
- Intravascular large B-cell lymphoma
- Immune hydrops fetalis
- Cat-scratch disease
- Calciphylaxis
- Arachnoiditis
- Primary cutaneous amyloidosis
- Heparin-induced thrombocytopenia
- Essential thrombocythemia
- Thalidomide embryopathy
- Madras motor neuron disease
- Duplication/inversion 15q11
- IgG4-related ophthalmic disease
- Zika virus disease
- Eosinophilic angiocentric fibrosis
- Pulmonary arteriovenous malformation
- Filariasis
- Lymphatic filariasis
- Isolated trigonocephaly
- Undifferentiated pleomorphic sarcoma
- Tracheal agenesis
- Limited systemic sclerosis
- Mounier-Kühn syndrome
- Sternal cleft
- Femur-fibula-ulna complex
- Toxocariasis
- Cleft palate
- Limited cutaneous systemic sclerosis
- Laryngotracheoesophageal cleft
- Median cleft lip/mandibule
- Progressive non-infectious anterior vertebral fusion
- Thymic epithelial neoplasm
- Eosinophilic gastroenteritis
- ALK-positive large B-cell lymphoma
- Truncus arteriosus
- Osteochondritis of tarsal/metatarsal bone
- African trypanosomiasis
- American trypanosomiasis
- Tuberculosis
- Systemic Epstein-Barr virus-positive T-cell lymphoproliferative disease of childhood
- Congenital bronchobiliary fistula
- Hydroa vacciniforme-like lymphoma
- Coronary arterial fistulas
- Trisomy X
- Triploidy
- Trisomy 13
- Trisomy 18
- Cole-Carpenter syndrome
- Silver-Russell syndrome due to 7p11.2p13 microduplication
- Silver-Russell syndrome due to an imprinting defect of 11p15
- Silver-Russell syndrome due to 11p15 microduplication
- Silver-Russell syndrome due to maternal uniparental disomy of chromosome 11
- Drug-induced lupus erythematosus
- Multiple system atrophy, parkinsonian type
- IgG4-related kidney disease
- Osteoclastic giant cell tumor of pancreas