Lipodystrophy

Symptom Information:

Symptom ID: HPO:0009125
Synonyms:
Lipodystrophy (disorder) [Orphanet:53200]
Lipodystrophy [Orphanet:53200]
Lipodystrophy [OMIM:Lipodystrophy]
Abnormal fat distribution/lipodystrophy [Orphanet:53200]
Lipodystrophy acquired [MedDRA:10049287]
Lipodystrophy [MedDRA:10049287]
Flat buttocks [MedDRA:10049287]
Peripheral lipodystrophy [MedDRA:10049287]
Lipodystrophy (in some patients) [OMIM:Lipodystrophy (in some patients)]
Lipodystrophies [MedDRA:10024606]
Quality:
Cross references:
HPO:0009064 "Generalized lipodystrophy" [Orphanet:53200]
Orphanet:53200 "Abnormal fat distribution/lipodystrophy" [Orphanet:53200]
OMIM: "Lipodystrophy" [OMIM:Lipodystrophy]
OMIM: "Lipodystrophy (in some patients)" [OMIM:Lipodystrophy (in some patients)]
UMLS:C0023787 "Lipodystrophy" [HPO:0009125]
UMLS:C0023787 "Lipodystrophy" [Orphanet:53200]
Is a (Direct Parents):
HPO         Abnormality of adipose tissue
Orphanet Build/stature/longevity anomalies
MedDRA Skin and subcutaneous tissue disorders NEC
Orphanet Abnormal subcutaneous fat tissue distribution
MedDRA Generalized lipodystrophy
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of connective tissue(HPO:0003549)
          Abnormality of adipose tissue(HPO:0009124)
             Lipodystrophy(HPO:0009125)
MedDRA:
Skin and subcutaneous tissue disorders(MedDRA:10040785)
    Skin and subcutaneous tissue disorders NEC(MedDRA:10040790)
       Generalized lipodystrophy(HPO:0009064)
          Lipodystrophy(HPO:0009125)
       Lipodystrophy(HPO:0009125)
Database Frequency: 54 / 7739
Resource:

All diseases associated with this symptom:

ACTH-dependent Cushing syndrome (Orphanet:99892)
ANALBUMINEMIA (OMIM:616000)
Alström syndrome (Orphanet:64)
Autosomal dominant cutis laxa (Orphanet:90348)
Autosomal recessive Emery-Dreifuss muscular dystrophy (Orphanet:98855)
Autosomal recessive cutis laxa type 2, classic type (Orphanet:357074)
Autosomal recessive cutis laxa type 2A (Orphanet:357058)
Becker nevus syndrome (Orphanet:64755)
Berardinelli-Seip congenital lipodystrophy (Orphanet:528)
Camurati-Engelmann disease (Orphanet:1328)
Carney complex (Orphanet:1359)
Congenital disorder of glycosylation (Orphanet:137)
Cushing disease (Orphanet:96253)
Cushing syndrome (Orphanet:553)
De Barsy syndrome (Orphanet:2962)
Dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome (Orphanet:2229)
Ehlers-Danlos syndrome, progeroid type (Orphanet:75496)
Encephalocraniocutaneous lipomatosis (Orphanet:2396)
Familial partial lipodystrophy associated with PPARG mutations (Orphanet:79083)
Familial partial lipodystrophy due to AKT2 mutations (Orphanet:79085)
Familial partial lipodystrophy, Dunnigan type (Orphanet:2348)
Familial partial lipodystrophy, Köbberling type (Orphanet:79084)
Familial symmetric lipomatosis (Orphanet:2398)
Focal dermal hypoplasia (Orphanet:2092)
Focal facial dermal dysplasia (Orphanet:79133)
Generalized congenital lipodystrophy with myopathy (Orphanet:228429)
Hutchinson-Gilford progeria syndrome (Orphanet:740)
Hypocalcemic vitamin D-resistant rickets (Orphanet:93160)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 1 (OMIM:608594)
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 2 (OMIM:269700)
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5 (OMIM:615238)
LIPODYSTROPHY, PARTIAL, ACQUIRED, WITH LOW COMPLEMENT COMPONENT C3,WITH OR WITHOUT GLOMERULONEPHRITIS (OMIM:613913)
Lipedema (Orphanet:77243)
Lipodystrophy - intellectual deficit - deafness (Orphanet:50811)
Lipodystrophy due to peptidic growth factors deficiency (Orphanet:1979)
Localized lipodystrophy (Orphanet:79088)
Mandibular hypoplasia-deafness-progeroid syndrome (Orphanet:363649)
Mandibuloacral dysplasia (Orphanet:2457)
Mandibuloacral dysplasia with type B lipodystrophy (Orphanet:90154)
Nakajo-Nishimura syndrome (Orphanet:2615)
Nasu-Hakola disease (Orphanet:2770)
PARTIAL LIPODYSTROPHY, CONGENITAL CATARACTS, AND NEURODEGENERATIONSYNDROME (OMIM:606721)
Partial acquired lipodystrophy (Orphanet:79087)
Primary lipodystrophy (Orphanet:90970)
Primary membranoproliferative glomerulonephritis (Orphanet:54370)
Progeria - short stature - pigmented nevi (Orphanet:2959)
Progeroid syndrome, Petty type (Orphanet:2963)
Proteus syndrome (Orphanet:744)
RUIJS-AALFS SYNDROME (OMIM:616200)
SHORT syndrome (Orphanet:3163)
STIFF SKIN SYNDROME (OMIM:184900)
Stiff skin syndrome (Orphanet:2833)
Werner syndrome (Orphanet:902)
Wrinkly skin syndrome (Orphanet:2834)