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Showing below up to 50 results in range #21,651 to #21,700.
- Thymidine phosphorylase deficiency (Q91159)
- Abscess of bone (Q91158)
- Dietary hypocalcaemia (Q91157)
- Bone granuloma (Q91156)
- Dihydroorotate dehydrogenase deficiency (Q91155)
- Autonomic nervous system of orbit (Q91154)
- Peripheral nerves of orbit (Q91153)
- Thymidine kinase 2 deficiency (Q91152)
- Other chronic osteomyelitis (Q91151)
- Septic osteonecrosis (Q91150)
- Hyper-beta-alaninaemia (Q91149)
- Candida paronychia (Q91148)
- Uridine-5'-monophosphate hydrolase superactivity (Q91147)
- Metastatic nasopharyngeal cancer [primary nasopharyngeal cancer spreading elsewhere] (Q91146)
- Salivary gland-type tumour of nasopharynx (Q91145)
- Dihydropyrimidinase deficiency (Q91144)
- Sequelae of dislocation, sprain or strain of joints or ligaments of shoulder girdle (Q91143)
- Dihydropyrimidine dehydrogenase deficiency (Q91142)
- Beta-ureidopropionase deficiency (Q91141)
- Congenital diverticular disease of small intestine (Q91140)
- Atypical ductal hyperplasia of breast (Q91139)
- Desmoid fibromatosis of breast (Q91138)
- Intestinal malrotation of small intestine (Q91137)
- Yolk sac tumour of the central nervous system (Q91136)
- Germinoma of the central nervous system (Q91135)
- Malignant germ cell tumour of pineal gland (Q91134)
- Mixed germ cell tumour of the central nervous system (Q91133)
- Duplication of small intestine (Q91132)
- Borderline phyllodes tumour of breast (Q91131)
- Intestinal agenesis (Q91130)
- Teratoma of brain (Q91129)
- Intracranial embryonal carcinoma (Q91128)
- Flat epithelial atypia of breast (Q91127)
- Choriocarcinoma of the central nervous system (Q91126)
- Atypical papilloma of breast (Q91125)
- Atypical lobular hyperplasia of breast (Q91124)
- Liver diseases due to disorders of carbohydrate metabolism (Q91123)
- Atypical teratoid rhabdoid tumour of brain (Q91122)
- Cranial neuropathy due to micronutrient deficiency (Q91121)
- Peripheral neuropathy due to multiple micronutrient deficiencies (Q91120)
- Maxillary or mandibular macrogenia (Q91119)
- Sensory polyneuropathy due to vitamin E deficiency (Q91118)
- Congenital spleen hypoplasia (Q91117)
- Other specified anomalies of jaw size (Q91116)
- Abdominal muscular injury (Q91115)
- 46,XY disorder of sex development due to 5-alpha-reductase 2 deficiency (Q91114)
- Leydig cell hypoplasia (Q91113)
- Mandibular hypoplasia (Q91112)
- Congenital malformation of spleen (Q91111)
- 46,XY disorder of sex development due to isolated 17, 20 lyase deficiency (Q91110)
