loading...| Preferred Name |
Amyloid Neuropathies, Familial |
|
| Synonyms |
Wohlwill-Andrade Syndrome |
|
| Definitions |
Inherited disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. The different clinical types based on symptoms correspond to the presence of a variety of mutations in several different proteins including transthyretin (PREALBUMIN); APOLIPOPROTEIN A-I; and GELSOLIN. |
|
| ID |
http://purl.bioontology.org/ontology/MESH/D028227 |
|
| altLabel |
Wohlwill-Andrade Syndrome Type I Familial Amyloid Polyneuropathy Familial Amyloid Polyneuropathy, Type I Familial Amyloid Polyneuropathy, Type II Familial Amyloid Neuropathy Portuguese Polyneuritic Amyloidosis British Type Amyloid Polyneuropathy Polyneuropathy, Familial Amyloid Polyneuritic Amyloidosis, Portuguese Wohlwill Corino Andrade Syndrome Familial Amyloid Polyneuropathy Amyloidoses, Portuguese Polyneuritic Hereditary Neuropathic Amyloidosis Wohlwill-Corino Andrade Syndrome Hereditary Neuropathic Amyloidoses Familial Amyloid Polyneuropathy, Type V Jewish Type Familial Amyloid Polyneuropathy Finnish Type Familial Amyloid Neuropathy Familial Amyloid Polyneuropathy, Type VI Familial Amyloid Polyneuropathy, Type III Amyloidoses, Hereditary Neuropathic Amyloid Polyneuropathy, British Type Amyloid Polyneuropathy, Iowa Type Amyloid Polyneuropathies, Familial Polyneuritic Amyloidoses, Portuguese Neuropathies, Familial Amyloid Neuropathic Amyloid Syndrome Familial Portuguese Polyneuritic Amyloidosis Type II Familial Amyloid Polyneuropathy Familial Amyloid Neuropathy, Finnish Type Amyloid Neuropathy Type 1 Familial Amyloid Neuropathy, Portuguese Type Amyloidosis, Portuguese Polyneuritic Familial Amyloid Neuropathies Neuropathy, Familial Amyloid Type III Familial Amyloid Polyneuropathy Familial Amyloid Polyneuropathy, Jewish Type Neuropathic Amyloidosis, Hereditary Neuropathic Amyloidoses, Hereditary Amyloid Neuropathy, Familial Familial Amyloid Polyneuropathy, Appalachian Type Familial Amyloid Polyneuropathies Iowa Type Amyloid Polyneuropathy Swiss Type Amyloid Polyneuropathy Wohlwill Andrade Syndrome Familial Amyloid Neuropathy, Andrade Type Appalachian Type Familial Amyloid Polyneuropathy Amyloid Syndromes, Neuropathic Amyloid Syndrome, Neuropathic Cerebral Amyloid Angiopathy, British Type Type IV Familial Amyloid Polyneuropathy Amyloidosis, Hereditary Neuropathic Polyneuropathies, Familial Amyloid Portuguese Type Familial Amyloid Neuropathy Type VI Familial Amyloid Polyneuropathy Portuguese Polyneuritic Amyloidoses Amyloid Polyneuropathy, Familial Neuropathic Amyloid Syndromes Familial Amyloid Polyneuropathy, Type IV Type V Familial Amyloid Polyneuropathy Amyloid Polyneuropathy, Swiss Type |
|
| AQL |
BL CF CI CL CO DG DH DI DT EC EH EM EN EP ET GE HI IM ME MI MO NU PA PC PP PS PX RH RT SU TH UR VE VI |
|
| cui |
C1527337 C0342608 C0268385 C0268384 C0268383 C0268386 C4551500 C0936273 C0155127 C0206245 |
|
| DC |
1 |
|
| definition |
Inherited disorders of the peripheral nervous system associated with the deposition of AMYLOID in nerve tissue. The different clinical types based on symptoms correspond to the presence of a variety of mutations in several different proteins including transthyretin (PREALBUMIN); APOLIPOPROTEIN A-I; and GELSOLIN. |
|
| DX |
20020101 |
|
| HN |
2002; use AMYLOID NEUROPATHIES 1994-2001; for FAMILIAL AMYLOID POLYNEUROPATHIES use AMYLOID NEUROPATHIES 1994-2001 |
|
| Inverse of AQ |
http://purl.bioontology.org/ontology/MESH/Q000097 http://purl.bioontology.org/ontology/MESH/Q000178 http://purl.bioontology.org/ontology/MESH/Q000175 http://purl.bioontology.org/ontology/MESH/Q000628 http://purl.bioontology.org/ontology/MESH/Q000276 http://purl.bioontology.org/ontology/MESH/Q000134 http://purl.bioontology.org/ontology/MESH/Q000139 http://purl.bioontology.org/ontology/MESH/Q000266 http://purl.bioontology.org/ontology/MESH/Q000378 http://purl.bioontology.org/ontology/MESH/Q000517 http://purl.bioontology.org/ontology/MESH/Q000662 http://purl.bioontology.org/ontology/MESH/Q000469 http://purl.bioontology.org/ontology/MESH/Q000150 http://purl.bioontology.org/ontology/MESH/Q000821 http://purl.bioontology.org/ontology/MESH/Q000191 http://purl.bioontology.org/ontology/MESH/Q000196 http://purl.bioontology.org/ontology/MESH/Q000473 http://purl.bioontology.org/ontology/MESH/Q000145 http://purl.bioontology.org/ontology/MESH/Q000382 http://purl.bioontology.org/ontology/MESH/Q000451 http://purl.bioontology.org/ontology/MESH/Q000453 http://purl.bioontology.org/ontology/MESH/Q000534 http://purl.bioontology.org/ontology/MESH/Q000532 http://purl.bioontology.org/ontology/MESH/Q000503 http://purl.bioontology.org/ontology/MESH/Q000188 http://purl.bioontology.org/ontology/MESH/Q000235 http://purl.bioontology.org/ontology/MESH/Q000201 http://purl.bioontology.org/ontology/MESH/Q000209 http://purl.bioontology.org/ontology/MESH/Q000208 http://purl.bioontology.org/ontology/MESH/Q000601 http://purl.bioontology.org/ontology/MESH/Q000000981 http://purl.bioontology.org/ontology/MESH/Q000652 |
|
| Machine permutation |
2002; see AMYLOID NEUROPATHIES 1994-2001; for FAMILIAL AMYLOID POLYNEUROPATHIES see AMYLOID NEUROPATHIES 1994-2001 |
|
| Mapped from | ||
| MDA |
20010725 |
|
| MMR |
20180228 |
|
| MN |
C16.320.565.176.050 C16.320.400.050 C10.668.829.050.050 C18.452.845.500.050.050 C18.452.648.176.050 C10.574.500.050 C18.452.845.500.075.050 |
|
| notation |
D028227 |
|
| prefLabel |
Amyloid Neuropathies, Familial |
|
| TERMUI |
T369831 T369833 T781871 T369834 T370130 T369832 T370125 T370131 T370099 T000938742 T369836 T370104 T370103 T370132 T370106 T781872 T369835 T370136 T370098 T370126 T370129 T370127 T370100 T370101 T370102 T781874 T370097 T751279 T053182 T750414 T370135 T053181 T370133 T370128 T370105 T370124 T781873 T370134 |
|
| TH |
OMIM (2013) NLM (2000) NLM (2012) NLM (2019) NLM (1994) NLM (2010) GHR (2014) ORD (2010) |
|
| tui |
T047 |
|
| subClassOf |
http://purl.bioontology.org/ontology/MESH/D017772 |