adolescent
http://www.orpha.net/ORDO/Orphanet_409947
From 12 to 18 years.
Term info
Term relations
Related from:
has_age_of_onset
- Pauci-immune glomerulonephritis without ANCA
- LRP5-related primary osteoporosis
- 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
- Autosomal recessive limb-girdle muscular dystrophy type 2Y
- 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
- Undifferentiated pleomorphic sarcoma
- Narcolepsy type 1
- Gastrocutaneous syndrome
- Dystonia-aphonia syndrome
- Early-onset schizophrenia
- Aquagenic palmoplantar keratoderma
- Proximal myopathy with focal depletion of mitochondria
- Thiel-Behnke corneal dystrophy
- Usher syndrome type 3
- Lymphedema-cerebral arteriovenous anomaly syndrome
- Epilepsy with myoclonic absences
- 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
- Wolfram syndrome
- Woodhouse-Sakati syndrome
- Autoimmune polyendocrinopathy type 1
- Palmoplantar keratoderma-esophageal carcinoma syndrome
- Hemophagocytic syndrome
- Rosaï-Dorfman disease
- Sea-blue histiocytosis
- Recurrent respiratory papillomatosis
- 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 deffect
- Autosomal dominant Charcot-Marie-Tooth disease type 2DD
- Carney-Stratakis syndrome
- Mayer-Rokitansky-Küster-Hauser syndrome
- Pancytopenia-developmental delay 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
- Atypical lichen myxedematosus
- Isochromosomy Yp
- Isochromosomy Yq
- Epithelioid sarcoma
- Sturge-Weber syndrome
- Phosphoribosylpyrophosphate synthetase superactivity
- Bipartite talus
- Cryopyrin-associated periodic syndrome
- Takayasu arteritis
- Hereditary thermosensitive neuropathy
- IRVAN syndrome
- Cone dystrophy with supernormal rod response
- Hemiparkinsonism-hemiatrophy syndrome
- Hereditary renal hypouricemia
- Pseudohypoparathyroidism type 1B
- Fatty acid hydroxylase-associated neurodegeneration
- Kufor-Rakeb syndrome
- Autosomal recessive ataxia due to PEX10 deficiency
- Hypergonadotropic hypogonadism-cataract syndrome
- Congenital pulmonary airway malformation
- Spastic ataxia with congenital miosis
- Cerebellar ataxia-hypogonadism syndrome
- Early-onset cerebellar ataxia with retained tendon reflexes
- Ménétrier disease