Insulin-resistant diabetes mellitus
Symptom Information:
Symptom ID: | HPO:0000831 | |||||||||||||||||
Synonyms: |
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Is a (Direct Parents): |
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Is a (Whole tree): |
HPO:
All(HPO:0000001) Phenotypic abnormality(HPO:0000118) Abnormality of the endocrine system(HPO:0000818) Diabetes mellitus(HPO:0000819) Insulin-resistant diabetes mellitus(HPO:0000831) Abnormality of metabolism/homeostasis(HPO:0001939) Abnormality of carbohydrate metabolism/homeostasis(HPO:0011013) Abnormal glucose homeostasis(HPO:0011014) Insulin resistance(HPO:0000855) Insulin-resistant diabetes mellitus(HPO:0000831) Diabetes mellitus(HPO:0000819) Insulin-resistant diabetes mellitus(HPO:0000831) MedDRA: Metabolism and nutrition disorders(MedDRA:10027433) Glucose metabolism disorders (incl diabetes mellitus)(MedDRA:10018424) Hyperglycaemic conditions NEC(MedDRA:10020638) Insulin-resistant diabetes mellitus(HPO:0000831) Diabetes mellitus(HPO:0000819) Insulin-resistant diabetes mellitus(HPO:0000831) |
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Database Frequency: | 22 / 7739 | |||||||||||||||||
Resource: |
All diseases associated with this symptom:
Alström syndrome | (Orphanet:64) |
Bangstad syndrome | (Orphanet:1227) |
Berardinelli-Seip congenital lipodystrophy | (Orphanet:528) |
CORTISONE REDUCTASE DEFICIENCY 2 | (OMIM:614662) |
Diabetes mellitus, ketosis-prone | (OMIM:612227) |
Familial partial lipodystrophy associated with PLIN1 mutations | (Orphanet:280356) |
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) |
Insulin-resistance syndrome type A | (Orphanet:2297) |
LIPODYSTROPHY, CONGENITAL GENERALIZED, TYPE 3 | (OMIM:612526) |
LIPODYSTROPHY, FAMILIAL PARTIAL, TYPE 5 | (OMIM:615238) |
Lipodystrophy due to peptidic growth factors deficiency | (Orphanet:1979) |
Mandibuloacral dysplasia | (Orphanet:2457) |
Mandibuloacral dysplasia with type A lipodystrophy | (Orphanet:90153) |
Mandibuloacral dysplasia with type B lipodystrophy | (Orphanet:90154) |
Mulibrey nanism | (Orphanet:2576) |
Partial acquired lipodystrophy | (Orphanet:79087) |
Rabson-Mendenhall syndrome | (Orphanet:769) |
Retinitis pigmentosa - intellectual deficit - deafness - hypogenitalism | (Orphanet:3085) |
SHORT syndrome | (Orphanet:3163) |