Category:Rare Diseases
From WikiMD's Food, Medicine & Wellness Encyclopedia
This is a category page. It lists all of the pages in category "Rare Diseases" as well as all subcategories of category "Rare Diseases" if any exist.
Pages in category "Rare Diseases"
The following 200 pages are in this category, out of 274 total.
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B
C
- Camptodactyly joint contractures facial skeletal dysplasia
- Camptodactyly-arthropathy-coxa vara-pericarditis syndrome
- Caudal regression syndrome
- CCA syndrome
- Chemke–Oliver–Mallek syndrome
- Choanal atresia deafness cardiac defects dysmorphia
- Chondrodysplasia punctata, Sheffield type
- Cleft lip palate mental retardation corneal opacity
- Cleft lip palate oligodontia syndactyly pili torti
- Cleft lip palate-tetraphocomelia
- Cogan syndrome
- Cole–Carpenter syndrome
- Congenital epulis
- Congenital hypoplastic anemia
- Cormier–Rustin–Munnich syndrome
- Corneal anesthesia deafness mental retardation
- Corticobasal syndrome
- Coxoauricular syndrome
- Cramer–Niederdellmann syndrome
- Craniometaphyseal dysplasia dominant type
- Craniosynostosis mental retardation heart defects
- Crawfurd syndrome
- Crouzonodermoskeletal syndrome
- Curry–Hall syndrome
D
- Deaf blind hypopigmentation
- Deafness hypospadias metacarpal and metatarsal syndrome
- Deaths from thrombotic thrombocytopenic purpura
- Dentin dysplasia
- Diaphragmatic agenesis radial aplasia omphalocele
- Diaphragmatic defect limb deficiency skull defect
- Diffuse neonatal hemangiomatosis
- Diprosopus
- Dipygus
- Distal arthrogryposis Moore–Weaver type
- Distal myopathy Markesbery–Griggs type
- Dupuytren subungual exostosis
- Dwarfism bluish sclerae
- Dwarfism mental retardation eye abnormality
- Dwarfism short limb absent fibulas very short digits
- Dwarfism stiff joint ocular abnormalities
- Dysplastic cortical hyperostosis
E
- Ectodermal dysplasia hypohidrotic autosomal dominant
- Ectodermal dysplasia Margarita type
- Ectodermal dysplasia mental retardation syndactyly
- Ectodermal dysplasia, hypohidrotic, autosomal recessive
- Ectopic ossification familial type
- Ectopic thymus
- Ectrodactyly-polydactyly syndrome
- Elisabeth Anderson Sierra
- Emery-Dreifuss syndrome
- Epidermolysis bullosa dystrophica, Bart type
- Epidermolysis bullosa, dermolytic
- Epidermolysis bullosa, junctional, Herlitz–Pearson
- Epiphyseal dysplasia dysmorphism camptodactyly
- Eprodisate disodium
- Erythrokeratodermia variabilis ichthyosis
- Extrasystoles short stature hyperpigmentation microcephaly
- Exudative retinopathy, familial
F
- Fetal akinesia syndrome X linked
- Fibrosing colonopathy
- Fibular hypoplasia scapulo pelvic dysplasia absent
- Flail limb
- Floating limb syndrome
- Focal facial dermal dysplasia
- Follicular atrophoderma
- Fraser-like syndrome
- Frias syndrome
- Frontonasal dysplasia phocomelic upper limbs
- Fryns–Fabry–Remans syndrome
G
- Gastritis, familial giant hypertrophic
- Gaucher-like disease
- Generalized trichoepithelioma
- Giedion syndrome
- Gigantism partial, nevi, hemihypertrophy, macrocephaly
- Glycogen
- Goniodysgenesis mental retardation short stature
- Gorlin Syndrome
- Growth deficiency brachydactyly unusual facies
- Growth mental deficiency syndrome of Myhre
- Growth retardation alopecia pseudoanodontia optic
H
- Hay–Wells syndrome recessive type
- Heart defect tongue hamartoma polysyndactyly
- Heide syndrome
- Hemangiopericytoma
- Hemifacial atrophy agenesis of the caudate nucleus
- Hemihypertrophy intestinal web corneal opacity
- Heparane sulfamidase deficiency
- Hereditary Multiple Exostoses
- Hirsutism congenital gingival hyperplasia
- Histiocyte Society
- Holmes–Collins syndrome
- HSN2
- Hutteroth–Spranger syndrome
- Hydrocephaly tall stature joint laxity
- Hypertrichosis congenital generalized X linked
- Hypertrophic hemangiectasia
- Hypertrophic osteoarthropathy, primary or idiopathic
- Hypoadrenocorticism hypoparathyroidism moniliasis
- Hypogonadotropic hypogonadism without anosmia, X linked
- Hypohidrotic ectodermal dysplasia with immune deficiency
- Hypoparathyroidism familial isolated
- Hypoparathyroidism short stature mental retardation
- Hypoplastic right heart microcephaly
I
K
L
M
- Mandibulofacial dysostosis-microcephaly syndrome
- Marfanoid craniosynostosis syndrome
- Markel–Vikkula–Mulliken syndrome
- Maroteaux–Fonfria syndrome
- Mastroiacovo–De Rosa–Satta syndrome
- McDowall syndrome
- Medeira Dennis Donnai syndrome
- Megalocornea mental retardation syndrome
- Meige's syndrome
- Menetrier's disease
- Menke-Hennekam syndrome
- Mental mixed retardation deafness clubbed digits
- Mental retardation anophthalmia craniosynostosis
- Mental retardation arachnodactyly hypotonia telangiectasia
- Mental retardation blepharophimosis obesity web neck
- Mental retardation cataracts calcified pinnae myopathy
- Mental retardation microcephaly phalangeal facial
- Mental retardation microcephaly unusual facies
- Mental retardation nasal hypoplasia obesity genital hypoplasia
- Mental retardation short stature absent phalanges
- Mental retardation short stature cleft palate unusual facies
- Mental retardation short stature deafness genital
- Mental retardation short stature hand contractures genital anomalies
- Mental retardation short stature hypertelorism
- Mental retardation short stature microcephaly eye
- Mental retardation short stature ocular and articular anomalies
- Mental retardation short stature scoliosis
- Mental retardation short stature unusual facies
- Mental retardation short stature wedge shaped epiphyses
- Mental retardation-polydactyly-uncombable hair
- Mesenteric panniculitis
- Metaphyseal dysostosis mental retardation conductive deafness
- Microcephalic primordial dwarfism
- Mirror hands feet nasal defects
- Mirror polydactyly-vertebral segmentation-limb defects syndrome
- Mmih syndrome
- Morgagni Stewart Morel syndrome
- Morgani–Turner–Albright syndrome
- Multiple pterygium syndrome lethal type
- Muscular dystrophy limb girdle type 2A, Erb type
- Muscular dystrophy limb-girdle autosomal dominant
- Muscular dystrophy limb-girdle with delta-sarcoglyan deficiency
- Myopathy tubular aggregates
O
- Ocular flutter
- Oculodental syndrome Rutherfurd syndrome
- Olivopontocerebellar atrophy type 1
- Onychotrichodysplasia and neutropenia
- Ophthalmomandibulomelic dysplasia
- Ophthalmoplegia mental retardation lingua scrotalis
- Optic atrophy ophthalmoplegia ptosis deafness myopia
- Osteoectasia familial
- Osteopathia condensans disseminata with osteopoikilosis
- Osteoporosis macrocephaly mental retardation blindness
- Osteosarcoma limb anomalies erythroid macrocytosis
