Category:Disease stubs
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Subcategories
This category has the following 3 subcategories, out of 3 total.
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Pages in category "Disease stubs"
The following 200 pages are in this category, out of 594 total.
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- Abrasion
- Absence of gluteal muscle
- Adult-onset immunodeficiency syndrome
- Alex Plank
- Alimentary toxic aleukia
- Amaurotic nystagmus
- Anomalous left coronary artery from the pulmonary artery
- Antenatal depression
- Anterior segment mesenchymal dysgenesis
- Aplasia
- Ari Ne'eman
- Asthma-COPD overlap
- Athelia (disease)
B
- Band keratopathy
- Benign paroxysmal vertigo of childhood
- Benjamin Burnley
- Berlin's edema
- Bietti's crystalline dystrophy
- Biliary hypoplasia
- Birdshot chorioretinopathy
- Blake Edwards
- Bleb (medicine)
- Blennorrhea
- Template:Blood-disease-stub
- Bogart–Bacall syndrome
- Bone dysplasia Moore type
- Boron deficiency (medicine)
- Brachymetapody anodontia hypotrichosis albinoidism
- Brachymorphism onychodysplasia dysphalangism syndrome
- Brachyolmia
- Briscoe Cain
C
- Caerns: Places of Power
- Calcinosis
- Camptodactyly joint contractures facial skeletal dysplasia
- Camptodactyly syndrome Guadalajara type 1
- Cantu–Sanchez–Corona–Fragoso syndrome
- Cantu–Sanchez–Corona–Garcia syndrome
- Cantu–Sanchez–Corona–Hernandes syndrome
- Carbamoyl phosphate synthetase I deficiency
- Cardiomyopathy, X linked, fatal infantile
- Carey–Fineman–Ziter syndrome
- Carnevale–Canun–Mendoza syndrome
- Carnevale–Krajewska–Fischetto syndrome
- Carpotarsal osteochondromatosis
- Carrión disease
- Cassia–Stocco–Dos Santos syndrome
- Castro–Gago–Pombo–Novo syndrome
- Cataract anterior polar dominant
- Cataract Hutterite type
- Cataract-microcornea syndrome
- Catastrophic illness
- Cerebellar hypoplasia endosteal sclerosis
- Cerebral calcification cerebellar hypoplasia
- Cerebral calcifications opalescent teeth phosphaturia
- Cerebroarthrodigital syndrome
- Chagas
- Charles' disease
- Childbirth-related post-traumatic stress disorder
- Chitayat–Haj–Chahine syndrome
- Chitayat–Meunier–Hodgkinson syndrome
- Chitty–Hall–Webb syndrome
- Chondrodysplasia pseudohermaphrodism syndrome
- Choroido cerebral calcification syndrome infantile
- Christian–Demyer–Franken syndrome
- Christian–Johnson–Angenieta syndrome
- Chromosome 1, monosomy 1p
- Chromosome 10, monosomy 10p
- Chromosome 10p terminal deletion syndrome
- Chromosome 17 trisomy
- Chromosome 18 long arm deletion syndrome
- Chromosome 18q deletion syndrome
- Chromosome 2, monosomy 2pter p24
- Chromosome 21 monosomy
- Chromosome 21, monosomy 21q22
- Chromosome 3 duplication syndrome
- Chromosome 4, monosomy distal 4q
- Chromosome 4, trisomy 4q25 qter
- Chromosome 6, monosomy 6p23
- Chromosome 6, monosomy 6q1
- Chromosome 6, monosomy 6q2
- Chromosome 7, monosomy 7q2
- Chromosome 7, trisomy mosaic
- Chudley–Lowry–Hoar syndrome
- Ciliary body melanoma
- Ciliary discoordination, due to random ciliary orientation
- Ciliary dyskinesia, due to transposition of ciliary microtubules
- Cilliers–Beighton syndrome
- Classic creutzfeldt-jakob disease
- Cleft lip palate deafness sacral lipoma
- Cleft lip palate mental retardation corneal opacity
- Coarse face hypotonia constipation
- Codesette syndrome
- Cohen–Lockood–Wyborney syndrome
- Colavita–Kozlowski syndrome
- Collins–Sakati syndrome
- Congenital heart disease ptosis hypodontia craniostosis
- Congenital heart disease radio ulnar synostosis mental retardation
- Template:Congenital-malformation-stub
- Conjugate gaze palsy
- Conjunctivitis
- Contractures ectodermal dysplasia cleft lip palate
- Cormier–Rustin–Munnich syndrome
- Corneal crystals myopathy neuropathy
- Corneal ectatic disorders
- Corsello–Opitz syndrome
- Cortada–Koussef–Matsumoto syndrome
- Cortical degeneration of the cerebellum parenchymatous
- Cote–Katsantoni syndrome
- Craniocervical instability
- Craniofaciocervical osteoglyphic dysplasia
- Craniomicromelic syndrome
- Craniosynostosis mental retardation clefting syndrome
- Crawfurd syndrome
- Criswick–Schepens syndrome
- Crossed polydactyly type 1
- Cryptomicrotia brachydactyly syndrome
- Cryptotia
- Curtis–Rogers–Stevenson syndrome
- Cutler Bass Romshe syndrome
- Cystic angiomatosis of bone, diffuse
- Cytopenia
- Cytoplasmic body myopathy
- Czeizel–Losonci syndrome
D
- Damian Milton
- Dandy–Walker facial hemangioma
- Dandy–Walker malformation postaxial polydactyly
- Davis–Lafer syndrome
- De Hauwere–Leroy–Adriaenssens syndrome
- Deafness hyperuricemia neurologic ataxia
- Deafness hypospadias metacarpal and metatarsal syndrome
- Deafness neurosensory pituitary dwarfism
- Dennis–Fairhurst–Moore syndrome
- Dermatoses induced by Personal Protective Equipment
- Developmental delay epilepsy neonatal diabetes
- Devriendt–Legius–Fryns syndrome
- Devriendt–Vandenberghe–Fryns syndrome
- Diaphragmatic agenesis radial aplasia omphalocele
- Dimitri–Sturge–Weber syndrome
- Diomedi–Bernardi–Placidi syndrome
- Dionisi–Vici–Sabetta–Gambarara syndrome
- Diplomatic illness
- Template:Disease-stub
- Distal arthrogryposis Moore–Weaver type
- Distal myopathy Markesbery–Griggs type
- Dominant zonular cataract
- Drachtman–Weinblatt–Sitarz syndrome
- Drag panic
- Duhring–Brocq disease
- Duker–Weiss–Siber syndrome
- Dupont–Sellier–Chochillon syndrome
- Dyggve–Melchior–Clausen syndrome
- Dyskeratosis congenita of Zinsser–Cole–Engman
- Dyssegmental dysplasia glaucoma
E
- Template:Ear-disease-stub
- Ectodermal dysplasia arthrogryposis diabetes mellitus
- Ectodermal dysplasia hypohidrotic hypothyroidism ciliary dyskinesia
- Ectodermal dysplasia Margarita type
- Ectodermal dysplasia tricho odonto onychial type
- Ectopia (medicine)
- Edwards–Patton–Dilly syndrome
- Elbow fracture
- Elliott–Ludman–Teebi syndrome
- Ellis–Yale–Winter syndrome
- Emedastine
- Emetophobia
- Engelhard–Yatziv syndrome
- Eosinophilic cryptitis
- Epidermolysis bullosa herpetiformis, Dowling–Meara
- Epidermolysis bullosa, junctional, Herlitz–Pearson
- Epiphyseal dysplasia dysmorphism camptodactyly
- Erasmo Moena
- Eric Morecambe
- Eronen–Somer–Gustafsson syndrome
- Erosive pustular dermatosis of the scalp
- Erythroderma lethal congenital
- Escher–Hirt syndrome
- Euhidrotic ectodermal dysplasia
- Eye defects arachnodactyly cardiopathy
- Template:Eye-disease-stub
- Eyebrows duplication syndactyly
F
- Facio skeletal genital syndrome Rippberger type
- Familial wilms tumor 2
- Faye–Petersen–Ward–Carey syndrome
- Feigenbaum–Bergeron–Richardson syndrome
- Fernhoff–Blackston–Oakley syndrome
- Fetal akinesia syndrome X linked
- Fetal brain disruption sequence
- Fibular hypoplasia scapulo pelvic dysplasia absent
- Fitzsimmons–McLachlan–Gilbert syndrome
- Flea (musician)
- Fluorometholone acetate
- Focal agyria pachygyria
- Follicular hamartoma alopecia cystic fibrosis
- Fontaine–Farriaux–Blanckaert syndrome
- Fowler–Christmas–Chapele syndrome
- Fragoso–Cid–Garcia–Hernandez syndrome
- Fraser-like syndrome
- Freire–Maia odontotrichomelic syndrome
- Friedel–Heid–Grosshans syndrome
