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MUMS:
List of Disorders
F - G
Number in parentheses indicates number of matches.
*
indicates there is a support group which covers that diagnosis.
FG Syndrome (17) *
FG Syndrome Home Page
Fabry Disease (3) *
Facial Cleft (4)
Facio-Auriculo-Vertebral Spectrum (Goldenhar Syndrome) (82) **
Facio-Scapulo-Humeral Dystrophy, Infantile (FSH) (3) *
Facioscapuloperoneal Dystrophy, Infantile (1)
Factor IV Deficiency (1)
Factor V Deficiency (2)
Factor XI Deficiency (1)
Factor XIII Deficiency (1)
Fahr's Disease (1)
Failure To Thrive (212)
Fainting Spells, Undiagnosed (3)
Familial Adenomatous Polyposis (Gardner Syndrome) (3)
Familial Dysautonomia (Riley-Day Syndrome) (8)**
www.fdhope.org/
Familial Erythrophagocytic Lymphohistiocytosis (1) *
Familial Exuderitive Vitrio (1)
Familial Intrahepatic Cholestasis (Liver Disease & Hearing Loss) (2)
Familial Mediteranean Fever (3)
Familial Spastic Diplegia (Paraparesis or Paraplegia) (7)
Fecal Retention Syndrome (following imperforate anus surgery) (3)
Feet & Hands Absent (1) *
Feet not growing (1)
Feingold Syndrome (Oculo-Digit-Esophageal-Duodenum (ODED) (2)
Femoral Antiversion (1)
Femoral Focal Deficiency, Proximal (PFFD) (10)*
Femoral Hypoplasia (23)*
Femoral Hypoplasia & Pierre Robin Syndrome (3)
Femoral Hypoplasia-Unusual Facies Syndrome (6)
Femur Absent (1)
Fetal Anticonvulsant Syndrome (14) Support Group: Email:
janet.oacs@btinternet.com>
Fetal Alcohol Syndrome/Affects (68) *
List of FAS Support Groups In U.S.
Fetal Brain Disruption Sequence (1)
Fetal Cocaine Syndrome (19)
Fetal Hydantoin Syndrome (Dilantin Syndrome) (7)
Fetal Hydantoin Syndrome & Tuberous Sclerosis (1)
Fetal Tegretol Syndrome (1)
Fetal Valproate Syndrome (6)
Fiber Type Disproportion, Congenital (11)
Fibillar Astrocytoma Hypothalmic Brain Tumor (1) *
Fibrodysplasia Ossificans Progressiva (Myositis Ossificans) (6) *
www.ifopa.org
Fibrolipomeningocele (form of Spina Bifida) (1)
Fibromatosis, Infantile (tumor in submadular gland) (1)
Fibromatosis, Juvenile Hyaline (3)*
Fibromyalgia (11) *
Fibromyostis & Reflex Sympathetic Dystrophy (1)
Fibrosarcoma, Infantile (1)
Fibula, Bilateral Abscence (2)
Fibula & Tibia Bowing, Posterior Medial (1)
Fibula Hemimelia Type III (missing leg) (2)
Fibular, Hemimelia, Congenital (8)
Fibular Hemimelia, Partial Type 1A (1)
Filippi Syndrome (4)*
Fingers, Abnormal (curved,short,tapered, w/pads, nubbins, etc.) (62)
Fingers, Clubbed (3)
Fingers, Nubbins (6)*
Fingers, Webbed (26)
Fingers, stopped growing (1)
Flavin(Trimethylaminuria) (Fish Odor Syndrome) (5)*
Flavoprotein Dehydrogenase Deficiency (subcategory of MADD) (1)
Floating Harbor Syndrome (3)*
Focal Segmential Glomerulosclerosis (scarred kidney tissue) (1)
Foot Absent (2) *
Foot Drop (7)
Forbes Disease (Glycogen Storage) (1) *
Forbes-Albright Syndrome (pituitary tumor) (1)
Forearm, Absence (13)
Forearm, Bilateral Absence (2)
Forearm, Shortened (8)*
Foreman Ovale Heart Defect (1)
Fragile X Syndrome (52)
www.fragilex.org
**
Fragile X Syndrome Carrier (repeat=64) (1)
Fraser Syndrome (6)
Freeman-Sheldon Syndrome (4) *
Frenulectomy (1)
Frey's Syndrome (Auriculotemporal) (1)
Fribillar Astrocytoma (hypothalmus tumor ) (1)
Friedreich's Ataxia (1) *
Frontoplagiocephaly (1)
Fructose 1/6 Dyphosphate Deficiency (2)
Fryns Syndrome (3)
Fused Eyelids (2)
G Syndrome (Opitz-Frias) (7)*
G-Tube Placement for feedings (761) *
www.oley.org
Gabali-Gonzales-Edwards Syndrome (1)
Gag reflex absent (8)
Gagging & Retching (9)
Galactosemia (15) **
Galactosidase Deficiency (1)
Galloway Syndrome (Microcephaly-Hiatus Hernia-Nephrosis Galloway Type(2)
Galloway-Mowat Syndrome (2)
Gang Raped (1)
Ganglioneuroblastoma (4)*
Gangliosidosis GM1 (14)
Gangliosidosis GM1 Type 1 (6)
Gangliosidosis GM1 Type II (4)
Gangliosidosis GM1, Type I and Stickler (1)
Gardner Syndrome (Familial Adenomatous Polyposis) (4)
Gastric Teratoma Tumor (1)
Gastroesophageal Reflux (476)
Gastroparesis (delayed gastric emptying) (3)
Gastroschisis (32)
Gaucher Disease (2) *
Gauche-Disease Type II (1)
Gaucher Disease Type III (1)*
Gelastic Seizures (laughing seizures) (1)
Genee-Wiedemann Syndrome (Miller Syndrome) (1) *
Genitals Retract & Swell (2)
Genital Warts (1)
Genito-Patella (absent scrotum & kneecaps) (1)
Gerstmann Syndrome (3)*
Gestational Trophoblastic Disease (1)
Giante Axonal Neuropahty (GAN) (2)
Giant Blouse Congenital Nevus (1 )
Giant Congenital Pigmented Nevis (1)*
Giant Melanocytic Hairy Nevus (4)*
Giardiasis Parasite Infection (3)
Gigantism (1)
Gilbert Syndrome (Pityriasis Rosea) (1)
Gillespie Syndrome (Aniridia/Cerebellum Ataxia MR Syndrome) (2)
Gitelman Syndrome (1)
Glanzmann's Thrombasthenia (6) 1 adult *
Glaucoma (32) *
Glaucoma, Congenital (9) *
Glioblastoma (1)
Glioblastoma Multiforme Spinal Cancer Stage IV (1)
Gliofibroma (Spinal Tumor-lower spine) (1)
Gliomatosis, Brain Cancer (1)
Glomerulonephritis Type III (Kidney Disease) (1) *
Glomerulonephritis, Membruno Proliferative Type II (MPGN) (1)*
Glomerulonephritis, Mesangial Proliferative (Kidney Disease) (1)*
Glomerulosclerosis, Focal Segmential (2)
Glottic Webbing (2)
Glucose Galactose Malabsorption Deficency (GGMD) (1)
Glucose-6-Phosphate Dehydrogenase Deficiency (G6PD) (1)
Glutaric Acidemia Type I (1) Spanish speaking
Glut1 Deficiency (1)
Glutaric Acidemia (19)
Glutaric Acidemia I (8)
www.ga1.freeservers.com
Glutaric Acidemia II (7) *
Glutaric Aciduria (7)*
Glutaric Aciduria Type 1 (3)*
Glutaric Aciduria Type II (4)*
Glutathione Synthetase Deficiency (1)
Glycogen Storage Disease (16)*
Glycogen Storage Disease Type O (1)*
Glycogen Storage Disease Type I (Von Gierke) (1)*
Glycogen Storage Disease Type IA (5) *
Glycogen Storage Disease Type II (Pompe's Disease) (2)*
Glycogen Storage Disease Type III (Forbes) (1)*
Glycogen Storage Disease Type IX (Phosphorylase B Kinase Deficiency) (1)*
Glycogen Storage Disease Type VII (2) *
Golabi-Rosen Syndrome (4)
Golabi-Rosen Syndrome (1)
Goldenhar Syndrome & Duane Syndrome (1)
Goldenhar Syndrome & Freys & Duane Syndrome (PAPVR) (1)
Goldenhar Syndrome & Holoprosencephaly Syndrome (1)
Goldenhar Syndrome & Klippel-Feil Syndrome (1)
Goldenhar Syndrome & Spina Bifida (Gulf War Effects) (2)
Goldenhar Syndrome & Treacher Collins (1)
Goldenhar Syndrome (Hemifacial Microsomia) (61) **
Goltz Syndrome (8)*
Goltz-Gorlin Syndrome (2)*
Gonadal Dysgenesis (1) *
Good Pasture Syndrome (destroyed kidneys) (1)
Gordon Syndrome (3)*
Gorlin-Chaudhry-Moss Syndrome (Gorlin Syndrome) (2)*
Gorlin-Goltz Syndrome (6)*
Granuloma Annulare (1)
Granulomatosis, Wegener's (1) *
Granulomatous Disease, Chronic (2) *
Gratification Phenomenon (1)
Graves Disease (4)*
Greig Cephalopolysyndactyly Syndrome (3)
Griscelli Syndrome (1)
http://home20.inet.tele.dk/griscellisyndrome
Group B Strep (5) *
Growth Hormone Deficiency (47) *
Growth Plate Abnormalities (8)
Guillain-Barre Syndrome (8) *
Gulf War Effects (22)*
Guttatepsorasis (1)
MUMS: National Parent to Parent Network
Julie Gordon
150 Custer Court
Green Bay, Wisconsin 54301-1243
1-877-336-5333 (Parents only please)
920-336-5333
1-920-339-0995 (fax)
E-mail:
mums@netnet.net
Web: http://www.netnet.net/mums/
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Last updated September 3, 2007
mums@netnet.net