changeset 8:38f0e68d1bac draft

Uploaded
author davidvanzessen
date Wed, 12 Aug 2015 05:39:09 -0400
parents a5233fbfc603
children 98a908a5cd2f
files OMT_coding.txt
diffstat 1 files changed, 1 insertions(+), 1 deletions(-) [+]
line wrap: on
line diff
--- a/OMT_coding.txt	Wed Aug 12 05:09:59 2015 -0400
+++ b/OMT_coding.txt	Wed Aug 12 05:39:09 2015 -0400
@@ -1,1 +1,1 @@
-1	1. Malformation
2	2. Deformation
3	3. Dysplasia
11	1A. Entire limb malformations
12	1B. Handplate malformations
21	Constriction ring sequence
22	Trigger digits
31	3A. Hypertrophy
32	3B. Tumorous conditions
110	1A. NOS entire limb malformation
111	1A1. Proximal-distal axis (entire limb)
112	1A2. Radio-ulnar axis (entire limb) 
113	1A3. Dorso-ventral axis (entire limb)
114	1A4. Unspecified axis (entire limb)
120	1B. NOS handplate malformation
121	1B1. Proximal-distal axis (hand)
122	1B2. Radio-ulnar axis (hand)
123	1B3. Dorso-ventral axis (hand)
124	1B4. Unspecified axis (hand)
210	Constriction ring sequence
220	Trigger digits
311	3A1. Whole limb hypertrophy
312	3A2. Partial Limb hypertrophy
321	3B1. Vascular tumors
324	3B4. Skeletal tumors
1100	1A. NOS malformation (entire limb)
1110	1A1. NOS prox-distal axis (entire limb)
1111	1A1i. Brachymelia
1112	1A1ii. Symbrachydactyly
1113	1A1iii. Transverse deficiency
1114	1A1iv. Intersegmental deficiency
1115	1A1v. Limb duplication
1120	1A2. NOS rad-uln axis (entire limb)
1121	1A2i. Radial longitudinal deficiency
1122	1A2ii. Ulnar longitudinal deficiency
1124	1A2iv. Radioulnar synostosis
1125	1A2v. Congenital radial head dislocation
1126	1A2vi. Humeroradial synostosis
1127	1A2vii. Madelung deformity
1131	1A3i. Dorsal dimelia (palmar nail)
1132	1A3ii. Ventral dimelia 
1141	1A4i. Abberant shoulder (incl Sprengel deformity)
1142	1A4ii. Arthrogryposis
1200	1B. NOS malformation (hand)
1211	1B1i. Brachydactyly
1213	1B1iii. Transverse deficiency (no arm involvement)
1220	1B2. NOS rad-uln axis malformation (hand)
1221	1B2i. Radial deficiency of the hand
1222	1B2ii. Ulnar deficiency of the hand
1223	1B2iii. Radial polydactyly
1224	1B2iv. Triphalangeal thumb
1225	1B2v. Ulnar dimelia
1226	1B2vi. Ulnar polydactyly
1232	1B3ii. Ventral dimelia (incl hypoplastic/aplastic nail)
1241	1B4i. Softi tissue malformations
1242	1B4ii. Sekeltal deficiencies
1243	1B4iii. Complex anomalies of unspecified axis (hand)
2100	Constriction ring sequence
2200	Trigger digits
3111	3A1i. Hemihypertrophy
3121	3A2i. Macrodactyly
3211	3B1i. Hemangioma
3212	3B1ii. Vascular malformation
3241	3B4i. Osteochondromatosis
3242	3B4ii. Echondromatosis
3244	3B4iv. Epiphyseal abnormalities
11000	1A. NOS entire limb malformation
11100	1A1. NOS proximal-distal axis malformation
11110	1A1i. Brachymelia
11121	1A1iia. Poland Syndrome
11130	1A1iii. Transverse deficiency
11140	1A1iv. Intersegmental deficiency
11150	1A1v. Limb duplication
11200	1A2. NOS rad-uln axis (entire limb)
11210	1A2i. Radial longitudinal deficiency
11220	1A2ii. Ulnar longitudinal deficiency
11240	1A2iv. Radioulnar synostosis
11250	1A2v. Congenital radial head dislocation
11260	1A2vi. Humeroradial synostosis
11270	1A2vii. Madelung deformity
11310	1A3i. Dorsal dimelia (palmar nail)
11320	1A3ii. Ventral dimelia 
11411	1A4ia. Sprengel deformity
11412	1A4ib. Abnormal shoulder muscles
11413	1A4ic. NOS shoulder malformation
11420	1A4ii. Arthrogryposis
12000	1B. NOS handplate malformation
12110	1B1i. Brachydactyly
12130	1B1iii. Transverse deficiency (no arm involvement)
12200	1B2. NOS rad-uln axis malformation (hand)
12210	1B2i. Radial deficiency of the hand
12220	1B2ii. Ulnar deficiency of the hand
12230	1B2iii. Radial polydactyly
12240	1B2iv. Triphalangeal thumb
12250	1B2v. Ulnar dimelia
12260	1B2vi. Ulnar polydactyly
12320	1B3ii. Ventral dimelia (incl hypoplastic/aplastic nail)
12411	1B4ia. Syndactyly
12412	1B4ib. Camptodactyly
12413	1B4ic. Thumb in palm deformity
12414	1B4id. Distal arthrogryposis
12421	1B4iia. Clinodactyly
12423	1B4iib. Synostosis/symphalangism
12431	1B4iiia. Complex syndactyly
12432	1B4iiib. Synpolydactyly
12433	1B4iiic. Cleft Hand
12434	1B4iiid. Apert Hand
21000	Constriction ring sequence
22000	Trigger digits
31110	3A1i. Hemihypertrophy
31210	3A2i. Macrodactyly
32110	3B1i. Hemangioma
32120	3B1ii. Vascular malformation
32410	3B4i. Osteochondromatosis
32420	3B4ii. Echondromatosis
32440	3B4iv. Epiphyseal abnormalities
\ No newline at end of file
+ID	name
1	1. Malformation
2	2. Deformation
3	3. Dysplasia
11	1A. Entire limb malformations
12	1B. Handplate malformations
21	Constriction ring sequence
22	Trigger digits
31	3A. Hypertrophy
32	3B. Tumorous conditions
110	1A. NOS entire limb malformation
111	1A1. Proximal-distal axis (entire limb)
112	1A2. Radio-ulnar axis (entire limb) 
113	1A3. Dorso-ventral axis (entire limb)
114	1A4. Unspecified axis (entire limb)
120	1B. NOS handplate malformation
121	1B1. Proximal-distal axis (hand)
122	1B2. Radio-ulnar axis (hand)
123	1B3. Dorso-ventral axis (hand)
124	1B4. Unspecified axis (hand)
210	Constriction ring sequence
220	Trigger digits
311	3A1. Whole limb hypertrophy
312	3A2. Partial Limb hypertrophy
321	3B1. Vascular tumors
324	3B4. Skeletal tumors
1100	1A. NOS malformation (entire limb)
1110	1A1. NOS prox-distal axis (entire limb)
1111	1A1i. Brachymelia
1112	1A1ii. Symbrachydactyly
1113	1A1iii. Transverse deficiency
1114	1A1iv. Intersegmental deficiency
1115	1A1v. Limb duplication
1120	1A2. NOS rad-uln axis (entire limb)
1121	1A2i. Radial longitudinal deficiency
1122	1A2ii. Ulnar longitudinal deficiency
1124	1A2iv. Radioulnar synostosis
1125	1A2v. Congenital radial head dislocation
1126	1A2vi. Humeroradial synostosis
1127	1A2vii. Madelung deformity
1131	1A3i. Dorsal dimelia (palmar nail)
1132	1A3ii. Ventral dimelia 
1141	1A4i. Abberant shoulder (incl Sprengel deformity)
1142	1A4ii. Arthrogryposis
1200	1B. NOS malformation (hand)
1211	1B1i. Brachydactyly
1213	1B1iii. Transverse deficiency (no arm involvement)
1220	1B2. NOS rad-uln axis malformation (hand)
1221	1B2i. Radial deficiency of the hand
1222	1B2ii. Ulnar deficiency of the hand
1223	1B2iii. Radial polydactyly
1224	1B2iv. Triphalangeal thumb
1225	1B2v. Ulnar dimelia
1226	1B2vi. Ulnar polydactyly
1232	1B3ii. Ventral dimelia (incl hypoplastic/aplastic nail)
1241	1B4i. Softi tissue malformations
1242	1B4ii. Sekeltal deficiencies
1243	1B4iii. Complex anomalies of unspecified axis (hand)
2100	Constriction ring sequence
2200	Trigger digits
3111	3A1i. Hemihypertrophy
3121	3A2i. Macrodactyly
3211	3B1i. Hemangioma
3212	3B1ii. Vascular malformation
3241	3B4i. Osteochondromatosis
3242	3B4ii. Echondromatosis
3244	3B4iv. Epiphyseal abnormalities
11000	1A. NOS entire limb malformation
11100	1A1. NOS proximal-distal axis malformation
11110	1A1i. Brachymelia
11121	1A1iia. Poland Syndrome
11130	1A1iii. Transverse deficiency
11140	1A1iv. Intersegmental deficiency
11150	1A1v. Limb duplication
11200	1A2. NOS rad-uln axis (entire limb)
11210	1A2i. Radial longitudinal deficiency
11220	1A2ii. Ulnar longitudinal deficiency
11240	1A2iv. Radioulnar synostosis
11250	1A2v. Congenital radial head dislocation
11260	1A2vi. Humeroradial synostosis
11270	1A2vii. Madelung deformity
11310	1A3i. Dorsal dimelia (palmar nail)
11320	1A3ii. Ventral dimelia 
11411	1A4ia. Sprengel deformity
11412	1A4ib. Abnormal shoulder muscles
11413	1A4ic. NOS shoulder malformation
11420	1A4ii. Arthrogryposis
12000	1B. NOS handplate malformation
12110	1B1i. Brachydactyly
12130	1B1iii. Transverse deficiency (no arm involvement)
12200	1B2. NOS rad-uln axis malformation (hand)
12210	1B2i. Radial deficiency of the hand
12220	1B2ii. Ulnar deficiency of the hand
12230	1B2iii. Radial polydactyly
12240	1B2iv. Triphalangeal thumb
12250	1B2v. Ulnar dimelia
12260	1B2vi. Ulnar polydactyly
12320	1B3ii. Ventral dimelia (incl hypoplastic/aplastic nail)
12411	1B4ia. Syndactyly
12412	1B4ib. Camptodactyly
12413	1B4ic. Thumb in palm deformity
12414	1B4id. Distal arthrogryposis
12421	1B4iia. Clinodactyly
12423	1B4iib. Synostosis/symphalangism
12431	1B4iiia. Complex syndactyly
12432	1B4iiib. Synpolydactyly
12433	1B4iiic. Cleft Hand
12434	1B4iiid. Apert Hand
21000	Constriction ring sequence
22000	Trigger digits
31110	3A1i. Hemihypertrophy
31210	3A2i. Macrodactyly
32110	3B1i. Hemangioma
32120	3B1ii. Vascular malformation
32410	3B4i. Osteochondromatosis
32420	3B4ii. Echondromatosis
32440	3B4iv. Epiphyseal abnormalities
\ No newline at end of file