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Showing below up to 50 results in range #27,701 to #27,750.
- Paraneoplastic disorders of the spinal cord (Q85109)
- Paraneoplastic autonomic neuropathy (Q85108)
- Autoimmune sensorimotor neuropathy (Q85107)
- Paraneoplastic neuromyopathy and neuropathy (Q85106)
- Vasculitis or vasculitic neuropathy (Q85105)
- Autoimmune motor neuropathy (Q85104)
- Paraneoplastic sensorimotor neuropathy (Q85103)
- Acquired tracheal deformity, not elsewhere classified (Q85102)
- Paraneoplastic sensory ganglionopathy (Q85101)
- Upper respiratory tract atrophy (Q85100)
- Cicatrix of trachea (Q85099)
- Trachea ossification (Q85098)
- Trachea compression (Q85097)
- Hypertrophic change of upper respiratory tract (Q85096)
- Tracheal adhesions (Q85095)
- Rhinoscleroma (Q85094)
- Olecranon bursitis related to prolonged pressure (Q85093)
- Leptospiral meningitis (Q85092)
- Necrotic trachea (Q85091)
- Leptospira interrogans infection (Q85090)
- Trachea collapse (Q85089)
- Stenosis of trachea, not elsewhere classified (Q85088)
- Ulceration of trachea (Q85087)
- Perichondritis of trachea (Q85086)
- Trachea stricture (Q85085)
- Leptospira infection of liver (Q85084)
- Other diseases of pharynx (Q85083)
- Tracheomalacia (Q85082)
- Abscess of trachea (Q85081)
- Obstruction of trachea (Q85080)
- Acquired tracheocele (Q85079)
- Trachea diverticulum (Q85078)
- Dyskinesia trachea (Q85077)
- Ceftriaxone-resistant Klebsiella pneumoniae (Q85076)
- Complement component C8 deficiency (Q85075)
- Deviation of trachea (Q85074)
- Calcification of trachea (Q85073)
- Complement component C5 deficiency (Q85072)
- Complement component C7 deficiency (Q85071)
- Crisponi syndrome (Q85070)
- Van den Ende-Gupta syndrome (Q85069)
- Complement component C9 deficiency (Q85068)
- Complement component C6 deficiency (Q85067)
- Marden-Walker syndrome (Q85066)
- Ceftazidime resistant Klebsiella pneumoniae (Q85065)
- Cefotaxime resistant Klebsiella pneumoniae (Q85064)
- Complete apical vaginal wall prolapse, Stage III (Q85063)
- Complete apical vaginal wall prolapse, Stage IV (Q85062)
- Neurogenic arthrogryposis multiplex congenita (Q85061)
- Hyper-IgM syndrome due to CD40 deficiency (Q85060)
