adiposogenitalE23.6

autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or BeckerG71.01

Becker's typeG71.01

cervical sympatheticG90.2

choroid H31.20

central areolarH31.22

choroideremiaH31.21

gyrate atrophyH31.23

specified type NECH31.29

cornea H18.50-

endothelialH18.51-

epithelialH18.52-

granularH18.53-

latticeH18.54-

macularH18.55-

specified type NECH18.59-

Duchenne's typeG71.01

due to malnutritionE45

Erb'sG71.02

Fuchs'H18.51-

Gower's muscularG71.01

hairL67.8

infantile neuraxonalG31.89

Landouzy-DéjérineG71.02

Leyden-Möbius, see also [Dystrophy, muscular, limb-girdle, by type]G71.039

meaning Limb girdle muscular dystrophy NOSG71.039

meaning Limb girdle muscular dystrophy, other specified type,, see [by type]

meaning Limb girdle muscular dystrophy, specified type NECG71.038

meaning Limb girdle muscular dystrophy type 2A G71.032

muscularG71.00

autosomal recessive, childhood type, muscular dystrophy resembling Duchenne or BeckerG71.01

benign G71.01

scapuloperoneal with early contractures [Emery-Dreifuss]G71.09

congenital G71.09

myotonicG71.11

distalG71.09

Duchenne typeG71.01

Emery-DreifussG71.09

Erb typeG71.02

facioscapulohumeralG71.02

Gower'sG71.01

hereditary , see also [Dystrophy, muscular, by type]G71.09

Landouzy-Déjérine typeG71.02

limb-girdleG71.039

alpha-sarcoglycan-relatedG71.0341

anoctamin-5-related autosomal recessive G71.035

autosomal recessive NECG71.038

beta-sarcoglycan-relatedG71.0342

calpain-3-relatedG71.032

autosomal dominantG71.031

autosomal recessiveG71.032

collagen VI related

autosomal dominantG71.031

autosomal recessiveG71.038

D1 G71.031

D2 G71.031

D3 G71.031

D4 G71.031

D5 G71.031

delta-sarcoglycan-relatedG71.0349

due to

alpha sarcoglycan dysfunctionG71.0341

anoctamin-5 dysfunctionG71.035

beta sarcoglycan dysfunctionG71.0342

fukutin related protein dysfunctionG71.038

sarcoglycan dysfunction, specified NECG71.0349

FKRP-related autosomal recessiveG71.038

gamma-sarcoglycan-relatedG71.0349

R1 G71.032

R2 G71.033

R3 G71.0341

R4 G71.0342

R5 G71.0349

R6 G71.0349

R7 G71.038

R8 G71.038

R9 G71.038

R10 G71.038

R11 G71.038

R12 G71.035

R13 G71.038

R14 G71.038

R15 G71.038

R16 G71.038

R17 G71.038

R18 G71.038

R19 G71.038

R20 G71.038

R21 G71.038

R22 G71.038

R23 G71.038

R24 G71.038

type 1 G71.031

type 1A G71.031

type 1B G71.031

type 1C G71.031

type 1E G71.031

type 1H G71.031

type 1I G71.031

type 2 G71.038

specified NECG71.038

type 2A G71.032

type 2B G71.033

type 2C G71.0349

type 2D G71.0341

type 2E G71.0342

type 2F G71.0349

type 2I G71.038

type 2L G71.035

myotonicG71.11

progressive , see also [Dystrophy, muscular, by type]G71.09

Charcot-Marie typeG60.0

pseudohypertrophic G71.01

scapulohumeralG71.02

scapuloperonealG71.09

severe G71.01

specified type NECG71.09

myocardium, myocardial, see [Degeneration, myocardial]

myotonic, myotonicaG71.11

nailL60.3

congenitalQ84.6

nutritionalE45

ocularG71.09

oculocerebrorenalE72.03

oculopharyngealG71.09

ovarianN83.8

polyglandularE31.8

reflex , see [Syndrome, pain, complex regional I]

retinal H35.50

in

lipid storage disordersE75.6

H36.89

systemic lipidosesE75.6

H36.89

involving

pigment epitheliumH35.54

sensory areaH35.53

pigmentaryH35.52

vitreoretinalH35.51

Salzmann's nodular, see [Degeneration, cornea, nodular]

scapuloperonealG71.09

skin NECL98.8

sympathetic , see [Syndrome, pain, complex regional I]

cervicalG90.2

tapetoretinalH35.54

thoracic, asphyxiatingQ77.2

unguiumL60.3

congenitalQ84.6

vitreoretinalH35.51

vulvaN90.4

yellow , see [Failure, hepatic]