Create issue ticket

145 Possible Causes for Hypoinsulinemic Hypoglycemia

  • Hypoinsulinemic Hypoglycemia and Body Hemihypertrophy

    DISEASE: Hypoinsulinemic hypoglycemia with hemihypertrophy Entry H01909 Disease Name Hypoinsulinemic hypoglycemia with hemihypertrophy Description Hypoinsulinemic hypoglycemia[genome.jp] Test Directory & Ordering - Clinical Synopsis HYPOINSULINEMIC HYPOGLYCEMIA WITH HEMIHYPERTROPHY; HIHGHH Custom clinical synopsis deleted successfully.[mnglabs.com] Hypoglycemia And Body Hemihypertrophy Hypoinsulinemic Hypoglycemia With Hemihypertrophy Isolated Hemihyperplasia Klippel-Trenaunay-Weber Syndrome Medullary Sponge Kidney[familydiagnosis.com]

  • Diabetes Mellitus Type 2

    AKT2 has also been implicated in a second disease, a type of hypoinsulinemic hypoglycemia ( OMIM:240900 ).[flybase.org]

  • 46,XY Gonadal Dysgenesis - Motor and Sensory Neuropathy Syndrome

    Hypoglycemia with Hemihypertrophy Hypospadias IMAGe syndrome IMAGe syndrome testing Infantile neuroaxonal dystrophy Infantile spasms Intellectual Disability IPEX syndrome[acronymattic.com] Callosum Hermansky Pudlak syndrome Holoprosencephaly Hutchinson-Gilford progeria syndrome (HGPS) Hydrocephalus hyperinsulinemia Hyperinsulinism Hypogonadotropic Hypogonadism Hypoinsulinemic[acronymattic.com]

  • Nonsyndromic Isolated Dilated Cardiomyopathy

    hypoglycemia and body hemihypertrophy Juvenile glaucoma LIG4 syndrome Lipoprotein glomerulopathy Mendelian susceptibility to mycobacterial diseases due to complete ISG15[csbg.cnb.csic.es] […] syndrome Hereditary breast and ovarian cancer syndrome Hereditary breast cancer Hereditary site-specific ovarian cancer syndrome Hyper-IgM syndrome type 2 Hyperlipidemia type 3 Hypoinsulinemic[csbg.cnb.csic.es]

  • Crouzon Syndrome-Acanthosis Nigricans Syndrome

    Hypoglycemia With Hemihypertrophy .[ukgtn.nhs.uk] 145981 Genetic Test Registry Hypochondroplasia HCH 146000 Genetic Test Registry Hypogonadotropic Hypogonadism 2 With Or Without Anosmia HH2 147950 Genetic Test Registry Hypoinsulinemic[ukgtn.nhs.uk]

  • Acromesomelic Dysplasia

    , familial, 5 INSR OMIM 3 146000 Hypochondroplasia FGFR3 OMIM 3 146110 Hypogonadotropic hypogonadism FGFR1 OMIM 3 240900 Hypoinsulinemic hypoglycemia with hemihypertrophy[gemdock.life.nctu.edu.tw] OMIM 3 613751 Heterotaxy, visceral, 4, autosomal ACVR2B OMIM 3 607685 Hypereosinophilic syndrome, idiopathic, resistant to imatinib PDGFRA OMIM 3 609968 Hyperinsulinemic hypoglycemia[gemdock.life.nctu.edu.tw]

  • Sensorineural Deafness with Dilated Cardiomyopathy

    hypoglycemia and body hemihypertrophy Juvenile glaucoma LIG4 syndrome Lipoprotein glomerulopathy Mendelian susceptibility to mycobacterial diseases due to complete ISG15[csbg.cnb.csic.es] […] syndrome Hereditary breast and ovarian cancer syndrome Hereditary breast cancer Hereditary site-specific ovarian cancer syndrome Hyper-IgM syndrome type 2 Hyperlipidemia type 3 Hypoinsulinemic[csbg.cnb.csic.es]

  • Solitary Fibrous Tumor

    Thus, the diagnosis of a non-islet cell tumor-induced hypoglycemia (NICTH) was established on the basis of the hypoinsulinemic hypoglycemia, the MSFT history, the presence[edmcasereports.com] hypoglycemia via dysregulated IGF-2 production.[endocrine.org] The diagnosis of NICTH is based on the findings of hypoinsulinemic hypoglycemia associated with the presence of big IGF2 (4) .[edmcasereports.com]

  • Macrocephaly

    Gene Prevalence Penetrance Clinical sensitivity Inheritance Condition AKT2 rare, unknown unknown unknown AD Hypoinsulinemic hypoglycemia with hemihypertrophy AKT3 rare, unknown[invitae.com] Intellectual disability syndrome with central obesity, macrocephaly and macrosomic features epiphyseal chondrodysplasia, Miura type ( ECDM ) Greig cephalopolysyndactyly syndrome hypoinsulinemic[invitae.com] hypoglycemia with hemihypertrophy Legius syndrome Lujan-Fryns syndrome Luscan-Lumish syndrome megalencephaly-polymicrogyria-polydactyly-hydrocephalus syndrome type 1 megalencephaly-polymicrogyria-polydactyly-hydrocephalus[invitae.com]

  • Congenital Deficiency in Alpha-fetoprotein

    hypoglycemia and body hemihypertrophy Cerebellar ataxia - hypogonadism Distal 22q11.2 microdeletion syndrome Familial thoracic aortic aneurysm and aortic dissection Hereditary[csbg.cnb.csic.es] […] thyroid carcinoma Posterior polar cataract Pulmonary venoocclusive disease Zonular cataract Bartsocas-Papas syndrome Familial partial lipodystrophy due to AKT2 mutations Hypoinsulinemic[csbg.cnb.csic.es]

Further symptoms