INDEX TO DISEASES
Jaundice
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J
Jaundice (yellow)--continued
Jaccoud's nodular fibrositis, chronic
catarrhal (acute)--continued
(Jaccoud's syndrome) 714.4
Jackson's
chronic 571.9
membrane 751.4
epidemic--see Jaundice, epidemic
paralysis or syndrome 344.8
cholestatic (benign) 782.4
veil 751.4
chronic idiopathic 277.4
Jacksonian
epidemic (catarrhal) 070.1
epilepsy 345.5
with hepatic coma 070.0
seizures (focal) 345.5
leptospiral 100.0
Jacob's ulcer (M8090/3)--see Neoplasm, skin, malignant,
spirochetal 100.0
by
febrile (acute) 070.1
site
with hepatic coma 070.0
Jacquet's dermatitis (diaper dermatitis) 691.0
leptospiral 100.0
Jadassohn's
spirochetal 100.0
blue nevus (M8780/0--see Neoplasm, skin, benign
fetus or newborn 774.6
disease (maculopapular erythroderma) 696.2
due to or associated with
intraepidermal epithelioma (M8096/0)
ABO
-- see Neoplasm, skin, benign
antibodies 773.1
Jadassohn-Lewandowski syndrome
incompatibility, maternal/fetal 773.1
(pachyonychia congenita) 757.5
isoimmunization 773.1
Jadassohn-Pellizari's disease (anetoderma).701.3
absence or deficiency of enzyme
Jadassohn-Tieche nevus (M8780/0-- see Neoplasm, skin,
system for bilirubin
benign
conjugation (congential) 774.39
Jaffe-Lichtenstein (-Uehlinger) syndrome 252.0
blood group incompatibility NEC 773.2
Jahnke's syndrome
breast milk inhibitors to conjugation 774.39
(encephalocutaneous
associated with preterm delivery 774.2
angiomnatosis) 759.6
bruising 774.1
Crigler-Najjar syndrome 277.4 [774.31]
Jakob-Creutzfeldt disease or syndrome 046.1
with dementia 290.10
delayed conjugation 774.30
Jaksch (-Luzet) disease or syndrome
associated with preterm delivery 774.2
(pseudoleukemia infantum) 285.8
development 774.39
Jamaican
drugs or toxins transmitted from mother 774.1
neuropathy 349.82
G-6-PD deficiency 282.2 [774.0]
paraplegic tropical ataxic-spastic syndrome 349.82
galactosemia 271.1 [774.5]
Janet's disease (psychasthenia) 300.89
Gilbert's syndrome 277.4 [774.31]
Janiceps 759.4
hepatocellular damage 774.4
Jansky-Bielschowsky amaurotic familial idiocy 330.1
hereditary hemolytic anemia (see
Japanese
also Anemia, hemolytic) 282.9 [774.0]
B type encephalitis 062.0
hypothyroidism, congential 243 [774.31]
river fever 081.2
incompatibility, maternal/fetal NEC 773.2
seven-day fever 100.89
infection 774.1
Jaundice (yellow) 782.4
inspissated bile syndrome 774.4
acholuric (familial) ( splenomegalic) (see also
isoimmunization NEC 773.2
Spherocytosis)
mucoviscidosis 277.01 [774.5]
282.0
acquired 283.9
breast milk 774.39
catarrhal (acute) 070.1
with hepatic coma 070.0
MD0753
C-2