orphafolder

| 100086 | Gallbladder neuroendocrine tumor
| 100101 | Neuroendocrine tumor with other location
| 100100 | Thymic tumor
| 100093 | Carcinoid syndrome
| 100092 | Gastroenteropancreatic neuroendocrine neoplasm
| 100094 | Multiple polyglandular tumor
| 100924 | Porphyria due to ALA dehydratase deficiency
| 100973 | FRAXE intellectual disability
| 100974 | FRAXF syndrome
| 100976 | Bathing suit ichthyosis
| 100054 | Hereditary angioedema type 3
| 100051 | Hereditary angioedema type 2
| 100057 | Renin-angiotensin-aldosterone system-blocker-induced angioedema
| 100056 | Acquired angioedema type 1
| 100055 | Acquired angioedema type 2
| 100069 | Semantic dementia
| 100070 | Progressive non-fluent aphasia
| 100067 | Waterhouse-Friderichsen syndrome
| 100073 | Neurogenic thoracic outlet syndrome
| 100075 | Neuroendocrine tumor of stomach
| 100071 | Mosaic trisomy 3
| 100078 | Ileal neuroendocrine tumor
| 100079 | Neuroendocrine neoplasm of appendix
| 100076 | Duodenal neuroendocrine tumor
| 100077 | Jejunal neuroendocrine tumor
| 100082 | Neuroendocrine tumor of anal canal
| 100083 | Laryngeal neuroendocrine tumor
| 100080 | Neuroendocrine tumor of the colon
| 100081 | Neuroendocrine tumor of the rectum
| 100020 | Refractory anemia with excess blasts type 2
| 100019 | Refractory anemia with excess blasts type 1
| 100022 | Extramedullary soft tissue plasmacytoma
| 100021 | Primary plasmacytoma of the bone
| 100024 | Mu-heavy chain disease
| 100026 | Gamma-heavy chain disease
| 100025 | Alpha-heavy chain disease
| 100032 | Hypocalcified amelogenesis imperfecta
| 100031 | Hypoplastic amelogenesis imperfecta
| 100034 | Hypomaturation-hypoplastic amelogenesis imperfecta with taurodontism
| 100033 | Hypomaturation amelogenesis imperfecta
| 100035 | Solitary necrotic nodule of the liver
| 100039 | Familial pseudohyperkalemia type 1
| 100043 | Autosomal dominant intermediate Charcot-Marie-Tooth disease type A
| 100044 | Autosomal dominant intermediate Charcot-Marie-Tooth disease type B
| 100045 | Autosomal dominant intermediate Charcot-Marie-Tooth disease type C
| 100046 | Autosomal dominant intermediate Charcot-Marie-Tooth disease type D
| 100047 | Esophageal duplication cyst
| 100048 | Tubular duplication of the esophagus
| 100049 | Primary interstitial lung disease specific to childhood due to pulmonary surfactant protein anomalies
| 100050 | Hereditary angioedema type 1
| 100016 | Lissencephaly with cerebellar hypoplasia type F
| 100015 | Lissencephaly with cerebellar hypoplasia type E
| 100012 | Lissencephaly with cerebellar hypoplasia type B
| 100011 | Lissencephaly with cerebellar hypoplasia type A
| 100014 | Lissencephaly with cerebellar hypoplasia type D
| 100013 | Lissencephaly with cerebellar hypoplasia type C
| 100008 | ACys amyloidosis
| 100003 | Intraneural perineurioma
| 100006 | ABeta amyloidosis, Dutch type
| 100000 | Reticular perineurioma
| 100001 | Sclerosing perineurioma
| 100002 | Extraneural perineurioma
| 99995 | Complex regional pain syndrome type 1
| 99991 | Relapsing epidemic typhus
| 99994 | Complex regional pain syndrome type 2
| 99989 | Intermediate DEND syndrome
| 99990 | Brill-Zinsser disease
| 99983 | Cutaneous myiasis
| 99981 | Apnea of prematurity
| 99978 | Klatskin tumor
| 99977 | Squamous cell carcinoma of the esophagus
| 99976 | Adenocarcinoma of the esophagus
| 99971 | Well-differentiated liposarcoma
| 99969 | Pleomorphic liposarcoma
| 99970 | Dedifferentiated liposarcoma
| 99967 | Myxoid/round cell liposarcoma
| 99965 | O'Sullivan-McLeod syndrome
| 99966 | Atypical teratoid rhabdoid tumor
| 99961 | Benign recurrent intrahepatic cholestasis type 2
| 99960 | Benign recurrent intrahepatic cholestasis type 1
| 99955 | Charcot-Marie-Tooth disease type 4B1
| 99956 | Charcot-Marie-Tooth disease type 4B2
| 99948 | Charcot-Marie-Tooth disease type 4A
| 99947 | Autosomal dominant Charcot-Marie-Tooth disease type 2A2
| 99950 | Charcot-Marie-Tooth disease type 4D
| 99949 | Charcot-Marie-Tooth disease type 4C
| 99952 | Charcot-Marie-Tooth disease type 4F
| 99951 | Charcot-Marie-Tooth disease type 4E
| 99954 | Charcot-Marie-Tooth disease type 4H
| 99953 | Charcot-Marie-Tooth disease type 4G
| 99940 | Autosomal dominant Charcot-Marie-Tooth disease type 2F
| 99939 | Autosomal dominant Charcot-Marie-Tooth disease type 2E
| 99942 | Autosomal dominant Charcot-Marie-Tooth disease type 2I
| 99941 | Autosomal dominant Charcot-Marie-Tooth disease type 2G
| 99944 | Autosomal dominant Charcot-Marie-Tooth disease type 2K
| 99943 | Autosomal dominant Charcot-Marie-Tooth disease type 2J
| 99946 | Autosomal dominant Charcot-Marie-Tooth disease type 2A1
| 99945 | Autosomal dominant Charcot-Marie-Tooth disease type 2L
| 99931 | Idiopathic pulmonary hemosiderosis
| 99932 | Heiner syndrome

« Previous 100 items Next 100 items » 1 ... 83 84 85 86 87 88 89 ... 97

Document Actions

Send this