ocular paralysis
51Congenital insensitivity to pain — Classification and external resources OMIM 243000 147430 DiseasesDB 31214 …
52Malignant hyperthermia — Classification and external resources Abnormalities in the Ryanodine receptor 1 gene are commonly detected in malignant hyperthermia ICD 10 T …
53Erythromelalgia — Classification and external resources Erythromelalgia in a 77 year old woman with longstanding polycythemia vera. ICD 10 I …
54Jervell and Lange-Nielsen syndrome — Classification and external resources ICD 9 426.82 OMIM 220400 DiseasesDB …
55Congenital absence of the vas deferens — Classification and external resources ICD 10 Q55.4 ICD 9 752.8 …
56Generalized epilepsy with febrile seizures plus — (GEFS+) is a syndromic autosomal dominant disorder where afflicted individuals can exhibit numerous epilepsy phenotypes.[1] GEFS+ can persist beyond early childhood (i.e., 6 years of age). GEFS+ is also now believed to encompass three other… …
57X-linked congenital stationary night blindness — Classification and external resources Malfunction in transmission from the photoreceptors in the outer nuclear layer to bipolar cells in the inner nuclear layer underlies CSNB. ICD …
58Erythrokeratodermia variabilis — Classification and external resources OMIM 133200 Erythrokeratodermia variabilis (also known as Erythrokeratodermia figurata variabilis, Keratosis extremitatum progrediens, Keratosis palmoplantaris transgrediens et progrediens, [1] …
59Vohwinkel syndrome — Classification and external resources OMIM 124500 DiseasesDB 32216 eMedicine …
60Oculodentodigital dysplasia — Classification and external resources OMIM 164200 DiseasesDB 32980 Oculodentodigital syndrome (ODD syndrome) is an extremely rare genetic conditio …