From 12 to 18 years.
This is just here as a test because I lose it
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- Pauci-immune glomerulonephritis without ANCA
- LRP5-related primary osteoporosis
- Refractory anemia
- Nodal marginal zone B-cell lymphoma
- Paroxysmal non-kinesigenic dyskinesia
- Paroxysmal exertion-induced dyskinesia
- Primary dystonia, DYT13 type
- Primary dystonia, DYT4 type
- Primary dystonia, DYT6 type
- Paroxysmal kinesigenic dyskinesia
- Hepatosplenic T-cell lymphoma
- TOR1AIP1-related limb-girdle muscular dystrophy
- Lemierre syndrome
- Grayson-Wilbrandt corneal dystrophy
- Pediatric collagenous gastritis
- Pseudoxanthoma elasticum-like skin manifestations with retinitis pigmentosa
- Progressive autosomal recessive ataxia-deafness syndrome
- Thiemann disease, familial form
- Madras motor neuron disease
- Pulmonary arteriovenous malformation
- Undifferentiated pleomorphic sarcoma
- Angiomatoid fibrous histiocytoma
- Narcolepsy type 1
- Gastrocutaneous syndrome
- Dystonia-aphonia syndrome
- Early-onset schizophrenia
- Aquagenic palmoplantar keratoderma
- Macrophage activation syndrome
- GJC2-related late-onset primary lymphedema
- Early-onset familial hypoaldosteronism
- Juvenile glaucoma
- Proximal myopathy with focal depletion of mitochondria
- Thiel-Behnke corneal dystrophy
- Usher syndrome type 3
- Lymphedema-cerebral arteriovenous anomaly syndrome
- Epilepsy with myoclonic absences
- Desminopathy
- X-linked myopathy with excessive autophagy
- Kikuchi-Fujimoto disease
- Autoimmune lymphoproliferative syndrome due to CTLA4 haploinsuffiency
- Schöpf-Schulz-Passarge syndrome
- Benign occipital epilepsy
- Hyperostosis corticalis generalisata
- Lissencephaly type 1 due to doublecortin gene mutation
- 46,XX ovotesticular disorder of sex development
- Wolfram syndrome
- Woodhouse-Sakati syndrome
- Autoimmune polyendocrinopathy type 1
- Palmoplantar keratoderma-esophageal carcinoma syndrome
- Hemophagocytic syndrome
- Rosaï-Dorfman disease
- Sea-blue histiocytosis
- Sinding-Larsen-Johansson disease
- Osgood-Schlatter disease
- Recurrent respiratory papillomatosis
- Autosomal dominant optic atrophy, classic form
- Malignant Sertoli-Leydig cell tumor of the ovary
- Maligant granulosa cell tumor of the ovary
- Malignant dysgerminomatous germ cell tumor of the ovary
- Familial cold urticaria
- Charcot-Marie-Tooth disease type 4G
- Charcot-Marie-Tooth disease type 4D
- Autosomal dominant Charcot-Marie-Tooth disease type 2L
- Autosomal dominant Charcot-Marie-Tooth disease type 2K
- Autosomal dominant Charcot-Marie-Tooth disease type 2G
- Autosomal dominant Charcot-Marie-Tooth disease type 2F
- Autosomal dominant Charcot-Marie-Tooth disease type 2D
- Autosomal dominant Charcot-Marie-Tooth disease type 2E
- Autosomal dominant Charcot-Marie-Tooth disease type 2B
- Autosomal dominant Charcot-Marie-Tooth disease type 2C
- Autosomal recessive axonal Charcot-Marie-Tooth disease due to copper metabolism defect
- Autosomal dominant Charcot-Marie-Tooth disease type 2DD
- Cardiogenic shock
- Czech dysplasia, metatarsal type
- Bronchial neuroendocrine tumor
- Carney-Stratakis syndrome
- Mayer-Rokitansky-Küster-Hauser syndrome
- Pleomorphic rhabdomyosarcoma
- Pancytopenia-developmental delay syndrome
- Senior-Loken syndrome
- Malignant peripheral nerve sheath tumor
- Satoyoshi syndrome
- Familial Scheuermann disease
- Autosomal dominant nocturnal frontal lobe epilepsy
- Spinocerebellar ataxia type 21
- Spinocerebellar ataxia type 5
- Spinocerebellar ataxia type 11
- Spinocerebellar ataxia type 27
- Spinocerebellar ataxia type 3
- Spinocerebellar ataxia type 6
- Idiopathic giant cell myocarditis
- Prader-Willi syndrome due to maternal uniparental disomy of chromosome 15
- Cap polyposis
- Juvenile overlap myositis
- AA amyloidosis
- Atypical lichen myxedematosus
- Isochromosomy Yp
- Isochromosomy Yq
- Enthesitis-related juvenile idiopathic arthritis