List of rare diseases-J
NIH genetic and rare disease info[edit source]
List of rare diseases-J is a rare disease.
- Jabs syndrome
- Jackhammer esophagus
- Jackson Barr syndrome
- Jackson-Weiss syndrome
- Jacobs syndrome
- Jacobs syndrome
- Jacobsen syndrome
- Jadassohn nevus phakomatosis
- Jadassohn-Tièche nevus
- Jadassohn-Tièche syndrome
- JAE
- Jaeken syndrome
- Jaffe Campanacci syndrome
- Jaffe-Campanacci syndrome
- Jaffer Beighton syndrome
- Jagell Holmgren Hofer syndrome
- Jail fever
- Jalili syndrome
- JALS
- Jamaican vomiting sickness
- Jancar syndrome
- Jankovic Rivera syndrome
- Jansen type metaphyseal chondrodysplasia
- Jansky-Bielschowsky disease
- Janz syndrome
- Japanese encephalitis
- Japanese type spondylometaphyseal dysplasia
- Jarcho-Levin syndrome
- JATD
- Jaw-winking
- JBS
- JBS
- JBTS1
- JBTS2
- JBTS3
- JBTS4
- JDM
- JE
- JEB
- JEB generalized intermediate
- JEB, generalized intermediate
- JEB-H
- JEB-Herlitz type
- JEB-I
- JEB-lo
- JEB-nH
- JEB-nH gen
- JEB-nH loc
- JEB-PA
- Jejunal atresia
- Jejunal atresia with renal adysplasia
- Jejunoileal atresia
- JEN-nH
- Jequier Kozlowski skeletal dysplasia
- Jequier-Kozlowski syndrome
- Jervell and Lange-Nielsen syndrome 2
- Jervell Lange-Nielsen syndrome
- Jessner disease
- Jessner-Kanof syndrome
- Jeune asphyxiating thoracic dystrophy
- Jeune syndrome
- Jeune syndrome situs inversus
- Jeune's syndrome
- JGCA
- JHD
- JHS
- JIP
- JLNS1
- JLNS2
- JME
- JMML
- JMP syndrome
- JMS
- JNP
- JOAG1
- Job syndrome autosomal dominant
- Johanson-Blizzard syndrome
- Johnson Munson syndrome
- Johnson neuroectodermal syndrome
- Johnson-Mcmillin syndrome
- Johnston Aarons Schelley syndrome
- Joint contractures - muscle atrophy - microcytic anemia - panniculitis-induced lipodystrophy
- Joint contractures with other abnormalities
- Joint contractures, hyperkeratosis, and severe hypoplasia of the posterior columns
- Joint instability syndrome
- Joint laxity, Familial
- Joint replacement infection
- Jones Hersh Yusk syndrome
- Jones syndrome
- Jonston's Alopecia- not a rare disease.
- Jorgenson Lenz syndrome
- JORRP (type)
- JOSeFINE
- Joubert syndrome
- Joubert syndrome 1
- Joubert syndrome 2
- Joubert syndrome 3
- Joubert syndrome 4
- Joubert syndrome 5
- Joubert syndrome with bilateral chorioretinal coloboma
- Joubert syndrome with congenital hepatic fibrosis
- Joubert syndrome with hepatic defect
- Joubert syndrome with ocular anomalies
- Joubert syndrome with oculorenal anomalies
- Joubert syndrome with oculorenal defect
- Joubert syndrome with orofaciodigital defect
- Joubert syndrome with renal anomalies
- Joubert syndrome with Senior-Loken syndrome
- Joubert-Boltshauser syndrome
- JP
- JPD
- JPG
- JPLS
- JPM
- JPMR
- JPS
- JS type B
- JS-H
- JS-OR
- Juberg Marsidi syndrome
- Juberg-Hayward syndrome
- Juberg-Hellman syndrome
- Juberg-Marsidi Intellectual disability syndrome
- Juberg-Marsidi syndrome
- Judge Misch Wright syndrome
- Jugular lymphatic obstruction sequence
- Jumping Frenchmen of Maine
- Junctional epidermolysis bullosa
- Junctional epidermolysis bullosa - pyloric atresia
- Junctional epidermolysis bullosa generalisata gravis
- Junctional epidermolysis bullosa generalisata mitis
- Junctional epidermolysis bullosa generalized intermediate
- Junctional epidermolysis bullosa inversa
- Junctional epidermolysis bullosa with pyloric atresia
- Junctional epidermolysis bullosa, Disentis type
- Junctional epidermolysis bullosa, generalized intermediate
- Junctional epidermolysis bullosa, Herlitz type
- Junctional epidermolysis bullosa, non-Herlitz type
- Jung Wolff Back Stahl syndrome
- Juvenile absence epilepsy
- Juvenile amyotrophic lateral sclerosis
- Juvenile arthritis- not a rare disease.
- Juvenile breast cancer (formerly)
- Juvenile breast carcinoma (formerly)
- Juvenile cataract, cerebellar atrophy, mental retardation, and myopathy
- Juvenile Charcot disease
- Juvenile chronic arthritis- not a rare disease.
- Juvenile cranial arteritis
- Juvenile dermatomyositis
- Juvenile enthesitis-related arthritis
- Juvenile giant cell arteritis
- Juvenile gigantomastia (subtype)
- Juvenile glaucoma with unusual upper lip and dental roots
- Juvenile hemochromatosis
- Juvenile hereditary epithelial dystrophy
- Juvenile hereditary hemochromatosis
- Juvenile Huntington disease
- Juvenile hyaline fibromatosis (former subtype)
- Juvenile idiopathic arthritis- not a rare disease.
- Juvenile intestinal polyposis
- Juvenile kyphosis
- Juvenile laryngeal papilloma
- Juvenile laryngeal papillomatosis (subtype)
- Juvenile Lou Gehrig disease
- Juvenile macular degeneration and hypotrichosis
- Juvenile macular dystrophy and congenital hypotrichosis
- Juvenile muscular atrophy of distal upper extremity (JMADUE)
- Juvenile muscular atrophy of distal upper limb
- Juvenile myelomonocytic leukemia
- Juvenile myoclonic epilepsy
- Juvenile myositis
- Juvenile nephronophthisis with Leber amaurosis
- Juvenile neuronal ceroid lipofuscinosis
- Juvenile onset HD
- Juvenile onset macular degeneration
- Juvenile onset pernicious anemia- not a rare disease.
- Juvenile ossifying fibroma
- Juvenile osteoporosis
- Juvenile Paget disease
- Juvenile Pagets disease
- Juvenile parkinsonism
- Juvenile pilocytic astrocytoma
- Juvenile PM
- Juvenile polyarthritis rheumatoid factor negative
- Juvenile polyarthritis rheumatoid factor positive
- Juvenile polymyalgia rheumatica
- Juvenile polymyositis
- Juvenile polyposis syndrome
- Juvenile primary lateral sclerosis
- Juvenile psoriatic arthritis
- Juvenile retinoschisis
- Juvenile rheumatoid arthritis- not a rare disease.
- Juvenile spondylarthropathy
- Juvenile spondyloarthropathy
- Juvenile sulfatidosis
- Juvenile temporal arteritis
- Juvenile-onset diabetes- not a rare disease.
- Juvenile-onset dystonia
- Juvenile-onset recurrent respiratory papillomatosis (type)
- Juvenile-onset small-fiber polyneuropathy
- Juvenile-onset vitelliform macular dystrophy
- Juxtafoveal retinal telangiectasia type 2- not a rare disease.
- JWS
NIH genetic and rare disease info[edit source]
List of rare diseases-J is a rare disease.
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