H00250  Congenital nongoitrous hypothyroidism (CHNG)
     H00408  Type 1 diabetes mellitus
     H00410  Maturity onset diabetes of the young (MODY)
     H01228  Insulin-resistant diabetes mellitus with acanthosis nigricans
     H00719  Leprechaunism
     H00942  Rabson-Mendenhall syndrome
     H01267  Familial hyperinsulinemic hypoglycemia
     H01388  Hyperprolactinemia
     H01294  Nephrogenic syndrome of inappropriate antidiuresis
     H00255  Hypogonadotropic hypogonadism
     H00253  Neurohypophyseal diabetes insipidus
     H02059  Leptin deficiency
     H02060  Leptin receptor deficiency
     H01193  Familial tumoral calcinosis
     H00967  Adiponectin deficiency
     H00214  Hypophosphatemic rickets
     H00240  Gitelman syndrome
     H01371  Hypercalcemia infantile
     H01293  Narcolepsy
     H00809  Familial epilepsy temporal lobe (ETL)
     H00265  Hereditary sensory and autonomic neuropathy
     H02674  Atrial standstill
     H00731  Atrial fibrillation
     H00801  Familial thoracic aortic aneurysm and dissection
     H00759  Waardenburg syndrome
     H01198  Fanconi renotubular syndrome
     H00243  Hyperkalemic distal renal tubular acidosis (RTA type 4)
     H00888  Nephrolithiasis/osteoporosis, hypophosphatemic
     H00512  Permanent neonatal diabetes mellitus
     H00910  Hirschsprung disease
     H02185  Spondylometaphyseal dysplasia
     H02543  Acromesomelic dysplasia
     H01884  Auriculocondylar syndrome
     H02679  Miura-type epiphyseal chondrodysplasia
     H02126  Mandibulofacial dysostosis with alopecia
     H00823  ABCD syndrome
     H02681  Short stature with nonspecific skeletal abnormalities