Wikipedia:WikiProject Missing encyclopedic articles/Missing diseases/2
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- Bagatelle Cassidy syndrome
- Baker Vinters syndrome
- Baksbat (broken courage) or Cambodian trauma syndrome [1]
- Baraitser Brett Piesowicz syndrome aka Pseudo-TORCH syndrome [2], OMIM had a page ([3]) but redirects it to [4]. The 3 authors have published about that one but not sure whether their names is a notable synonum of that disease.
- Baraitser Rodeck Garner syndrome [5], [6]
- Barnicoat Baraitser syndrome
- Barrow Fitzsimmons syndrome
- Basal cell nevus anodontia abnormal bone mineralization
- Basaran Yilmaz syndrome [7]
- Basedow's coma [8]
- Battaglia Neri syndrome [9]
- Bazopoulou Kyrkanidou syndrome aka Craniofaciocervical osteoglyphic dysplasia
- Beemer Ertbruggen syndrome [10], [11]
- Behrens Baumann Dust syndrome [12]
- Bellini Chiumello Rinoldi syndrome --Mispelling of--> Bellini Chiumello Rimoldi syndrome [13] as shown here: [14] (see author's name).
- Ben Ari Shuper Mimouni syndrome [15]
- Benallegue Lacete syndrome [16]
- Bencze syndrome aka Hemifacial hyperplasia strabismus [17]
- Berry aneurysm, cirrhosis, pulmonary emphysema, and cerebral calcification - [18], [19]
- Bidirectional tachycardia - [20]
- Biliary hypoplasia [21]
- Billard Toutain Maheut syndrome aka Familial developmental dysphasia, FOXP2-associated dysphasia
- Billet Bear syndrome [22]
- Bindewald Ulmer Muller syndrome [23], [24] Fallot complex
- Bixler Christian Gorlin syndrome aka HMC syndrome [25], [26]
- Blaichman syndrome [27]
- Blepharo cheilo dontic syndrome aka BCD syndrome, Blepharocheilodontic syndrome Elschnig syndrome [28], [29]
- Blepharo facio skeletal syndrome [30]
- Blepharoptosis aortic anomaly [31] (Main article is in Ptosis (eyelid)
- Blepharoptosis cleft palate ectrodactyly dental anomalies [32]
- Blethen Wenick Hawkins syndrome [33]
- BOD syndrome --Short for--> Brachymorphism-onychodysplasia-dysphalangism syndrome [34]
- Bone dysplasia corpus callosum agenesis [35]
- Bone dysplasia lethal Holmgren type [36]
- Bone dysplasia Moore type [37]
- Bone marrow failure neurologic abnormalities
- Bonneau-Beaumont syndrome [38]
- Bonneman Meinecke Reich syndrome [39]
- Book syndrome --also known as--> PHC syndrome or Premolar aplasia, hyperhidrosis, and canities prematura syndrome [40]
- Bork Stender Schmidt syndrome
- Boscherini Galasso Manca Bitti syndrome [41]
- Boylan Dew Greco syndrome [42]
- Brachioskeletogenital syndrome --also known as--> BSG syndrome [43]
- Brachycephalofrontonasal dysplasia
- Brachydactylous dwarfism Mseleni type
- Brachydactyly anonychia
- Brachydactyly dwarfism mental retardation
- Brachydactyly mesomelia mental retardation heart defects
- Brachydactyly scoliosis carpal fusion
- Brachydactyly small stature face anomalies
- Brachydactyly tibial hypoplasia
- Brachymesomelia renal syndrome
- Brachymetapody anodontia hypotrichosis albinoidism
- Brachymorphism onychodysplasia dysphalangism syndrome
- Brachyolmia recessive Hobaek type
- Brachyolmia
- Braddock Carey syndrome
- Brunoni syndrome
- Bullous dystrophy macular type
- Burn Goodship syndrome
- CAHMR syndrome
- Calloso genital dysplasia
- Calvarial hyperostosis
- Campomelia Cumming type
- Camptodactyly fibrous tissue hyperplasia skeletal dysplasia
- Camptodactyly joint contractures facial skeletal dysplasia
- Camptodactyly syndrome Guadalajara type 1
- Camptodactyly syndrome Guadalajara type 2
- Camptodactyly vertebral fusion
- Cantalamessa Baldini Ambrosi syndrome
- Caratolo Cilio Pessagno syndrome
- Carbon baby syndrome
- Cardioauditory syndrome of Sanchez- Cascos
- Cardioauditory syndrome
- Cardiofacial syndrome short limbs
- Cardiomelic syndrome Stratton Koehler type
- Cardiomyopathy cataract hip spine disease
- Cardiomyopathy, fatal fetal, due to myocardial calcification
- Cardiomyopathy, X linked, fatal infantile
- Carpal deformity migrognathia microstomia
- Carpenter Hunter type
- Carpotarsal osteochondromatosis
- Cataract aberrant oral frenula growth retardation
- Cataract anterior polar dominant
- Cataract congenital Volkmann type
- Cataract congenital with microphthalmia
- Cataract Hutterite type
- Cataract hypertrichosis mental retardation
- Cataract mental retardation hypogonadism
- Cataract skeletal anomalies
- Cataract,congenital ichthyosis
- Cataract-glaucoma
- Caudal appendage deafness
- Ccge syndrome
- CDK4 linked melanoma
- Cecato De lima Pinheiro syndrome
- Celiac disease epilepsy occipital calcifications
- Cennamo Gangemi syndrome
- Cerebellar ataxia ectodermal dysplasia
- Cerebellar hypoplasia endosteal sclerosis
- Cerebellar hypoplasia tapetoretinal degeneration
- Cerebellar parenchymal degeneration
- Cerebelloparenchymal disorder 3
- Cerebellum agenesis hydrocephaly
- Cerebral calcification cerebellar hypoplasia
- Cerebral calcifications opalescent teeth phosphaturia
- Cerebral malformations hypertrichosis claw hands
- Cerebral ventricle neoplasm
- Cerebro oculo dento auriculo skeletal syndrome -AKA: CODAS syndrome (from [44] and [45]
- Cerebro oculo genital syndrome -AKA: Duker-Weiss-Siber syndrome (from [46]).
- Cerebro oculo skeleto renal syndrome -AKA: Silengo-Lerone-Pelizzo syndrome (from [47]).
- Cerebroarthrodigital syndrome -[48][49]
- Cervical hypertrichosis neuropathy [50] [51] (same linking as one below?)
- Cervical hypertrichosis peripheral neuropathy [52] [53]
- Cervical ribs sprengel anomaly polydactyly [54] [55]
- Charles' Disease
- Charlie M syndrome [56]
- Chemke Oliver Mallek syndrome [57]
- Chitayat Haj Chahine syndrome
- Chitayat Moore Del Bigio syndrome [58]
- Chitty Hall Baraitser syndrome [59] [60]
- Chitty Hall Webb syndrome [61] [62]
- Chlamydial and Gonococcal Conjunctivitis
- Choanal atresia deafness cardiac defects dysmorphia [63]
- Choledochal cyst, hand malformation [64]
- Cholestasis pigmentary retinopathy cleft palate is it referring to Hardikar syndrome? [65]
- Chondrodysplasia lethal recessive or Recessive lethal chondrodysplasia [66]
- Chondrodysplasia pseudohermaphrodism syndrome --also known as-->Pseudohermaphrodism and chondrodysplasia,[[67]] [68]
- Chondrodysplasia punctata with steroid sulfatase deficiency
- Chondrodysplasia situs inversus imperforate anus polydactyly [69]
- Chondromatosis (benign)
- Chondrodysplasia punctata, humero-metacarpal type [70][71]
- Choreoacanthocytosis amyotrophic [72], [73]
- Chorioretinopathy dominant form microcephaly
- Choroidal atrophy alopecia--also known as--> Moloney syndrome or Regional choroidal atrophy and alopecia. Symptoms include: Fine hair, absent/decreased lashes, absent/decreased eyebrows, visual loss-mild/suspected, dysplastic/thick/grooved toenails and fingernails. [74]
- Choroido cerebral calcification syndrome infantile
- Christian Demyer Franken syndrome [75]
- Christian Johnson Angenieta syndrome [76]
- Christianson Fourie syndrome