Patient Information

To reset the search terms or the alphabet filter, just click "Patient Information" in the menu again, and start fresh.

3 | A | B | C | D | E | F | G | H | I | J | K | L | M | N | O | P | R | S | T | U | V | W | Z

Patient Handout Title
Gracile Bone Dysplasia
Gurrieri Syndrome
Gyrate Atrophy
Hallermann-Streiff Syndrome
Harboyan Syndrome
Heart and Brain Malformation Syndrome
Heimler Syndrome 1
Heimler Syndrome 2
HELIX Syndrome
Hereditary Mucoepithelial Dysplasia
Hermansky-Pudlak Syndrome
Histiocytic Dermatoarthritis
Homocystinuria, Beta-Synthase Deficiency
Homocystinuria, MTHFR Deficiency
Hoyeraal-Hreidarsson Syndrome
Hunter Syndrome (MPS II)
Hurler and Scheie Syndromes (MPS IH, IS, IH/S)
Hyperferritinemia-Cataract Syndrome
Hyperoxaluria, Primary, Type I
Hyperphosphatasia with Mental Retardation Syndrome 6
Hypoparathyroidism, Familial Isolated
Hypotonia, Infantile, with Psychomotor Retardation
Hypotonia, Infantile, with Psychomotor Retardation And Characteristic Facies 1
Hypotonia, Infantile, with Psychomotor Retardation And Characteristic Facies 2
Hypotonia, Infantile, with Psychomotor Retardation and Characteristic Facies 3

You are here