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MUMS: List of Disorders - "A"

MUMS:
List of Disorders
A

Number in parentheses indicates number of matches.
* indicates there is a support group which covers that diagnosis.

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  • C-PAP (14)
  • Cachexia (1)
  • Caffey Disease (Cortical Hyperostosis, Infantile) (2)
  • Caffey-Silverman Syndrome (1)
  • CATCH 22 Syndrome(DiGeorge+Velo-Cardio-Facial+Conotruncal) (5) *
  • Calcium Deficiency (26)
  • Calcium Levels Too High (1)
  • Campomelic Dysplasia Syndrome (11) *
  • Camptodactyly (5)
  • Canavan's Leukodystrophy (3) * www.canavan.org/
  • Cancer (135) * www.cancer.org and www.candlelighters.org
  • Cancer, Acute Lymphatic Leukemia (ALL) (6)*
  • Cancer, Anoplastic Oligodendroglioma Tumor (1)
  • Cancer, Chordoma (Spinal Tumor) (1) *
  • Cancer, Ewings Sarcoma (6) *
  • Cancer, Nasopharyngeal (1) *
  • Cancer, Ovaries (1) *
  • Cancer, Primary Neuroectodermal Tumor of the Spine (PNET) (2) *
  • Cancer, Rhabdomyosarcoma (4)*
  • Cancer, Yolk Sac Tumor (Germcell) (1) *
  • Candida Yeast Infection (7)
  • Candida Yeast Infection in Large Intestine (1)
  • Carbamyl Phosphate Synthetase Deficiency (CPS) (2) *
  • Carbohydrate-Deficient Glycoprotein Syndrome (CDGS) (8) *
  • Carbon Monoxide Poisoning (2)
  • Cardiac Pacemaker (23)
  • Cardio-Facio-Cutaneous Syndrome (19) **
  • Cardiomyopathy (36) * www.childrenscardiomyopathy.org
  • Cardiomyopathy, Idiopathic Hypertrophic (18) **
  • Cardiomyopathy, Idiopathic Restrictive (1)
  • Carey-Fineman-Ziter Syndrome (Moebius & Pierre Robin) (2)
  • Carnitine Deficiency Syndrome, Hereditary (20) **
  • Carnitine Palmityltransferase Deficiency (CPT) (3) *www.fodsupport.org
  • Carnitine Palmityltransferase Deficiency (CPT) Type II (1) *www.fodsupport.org
  • Carnosinase Deficiency & Chromosome 18q- (1)
  • Carpal Tunnel Syndrome (5)*
  • Carpenter Syndrome (5) *
  • Cartilage-Hair-Hypoplasia Syndrome (McKusick Syndrome) (4)*
  • Cat Eye Syndrome (Chromosome 22, partial Trisomy) (9)
  • Cat's Cry Syndrome (Cri du Chat, 5p-) (39) *
  • Cataplexy (2)
  • Cataracts (68) *
  • Caudal Regression Syndrome (17)
  • Caudal Regression Syndrome & Pierre Robin (1)
  • Caudal Regression Syndrome & Sacral Agenesis (10)
  • Cavernous Hemangioma (9)*
  • Cd5 - Cd19 PID, Primary Immune Deficiency (1)
  • Cayman Type Ataxia (1)
  • Cecostomy (1)
  • Celiac & Down Syndrome (3)
  • Celiac Disease (16) *
  • Celiac Sprue (16) *
  • Central Abdominal Raphe Syndrome with Hemangiomas of the Face (1)
  • Central Apnea Anomoly Innominate Artery Syndrome (1) **
  • Central Auditory Processing Disorder (CAPD) (2)
  • Central Core Disease (6) *
  • Central Hypoventilation Syndrome, Congenital (9) **
  • Central Nervous System Disorder (10)
  • Centronuclear Myopathy (Myotubular Myopathy) (15) **
  • Cerebellar Ataxia, Acute, (Post Infectious Cerebelitis) (1)
  • Cerebellar Hemangioblastoma (2)
  • Cerebellar Hypoplasia (23)
  • Cerebellar Pontine Hypoplasia (2)
  • Cerebellar Vermis Agenesis (10)
  • Cerebellar Vermis Hypoplasia (5)
  • Cerebral Atrophy (20)
  • Cerebral Giantism (10)
  • Cerebral Palsy (1585) * CP Websites
  • Cerebral Palsy & Blindness (103)
  • Cerebral Palsy & Deaf-Blind (13)
  • Cerebral Palsy & Deafness (32)
  • Cerebral Palsy & Hearing Impaired (96)
  • Cerebral Palsy & Hydrocephalus (101)
  • Cerebral Palsy & Vision Disorders (230) *
  • Cerebral Palsy, Hemiparesis (one side of the body involved) (35)* www.hemikids.org
  • Cerebral Palsy, Choreoathatoid (9)*
  • Cerebral Palsy, Chorea Hyperkenetic Pyramidal (1)
  • Cerebral Palsy, Triplegia (3)
  • Cerebro-Costo-Mandibular Syndrome (5)
  • Cerebro-Costo-Mandibular Syndrome & Hypoplastic Left Heart (1)
  • Cerebro-Hepato-Renal Syndrome (Zellweger) (11)*
  • Cerebro-Oculo-Facio-Skeletal Syndrome (Pena-Shokier II) (6)
  • Cervical Cancer (1)
  • Cervical Myelopathy (Spinal Cord Injury) (1)
  • Cervical Spinal Cord Cyst (Hydromelia) (1) *
  • Cervical Spinal Cord Injury (1) *
  • Cervicoculofacial Dysplasia (Cervico-Oculo-Acoustic) (2)
  • Cervico-Oculo-Acoustic (Wildervanck Syndrome) (2)
  • Citrullinemia (Citrulluria) Urea Cycle Disorder (4) *
  • Charcot-Marie-Tooth Disease (21) **
  • CHARGE Syndrome & Tetralogy of Fallot (4)
  • CHARGE Syndrome (49) *
  • CHARGE-VATER Syndrome (2)
  • Cheilitis Granulomatosa (1)
  • Childhood Ataxia with Acute CNS Hypomyelination (CACH) (a Leukodystrophy)(2)
  • Choanal Atresia (26)
  • Cholangitis, Primary Sclerosing (1)
  • Cholestasis (Liver Disease) (3)
  • Cholesteoma (1)
  • Cholesterol, Cannot produce (1)
  • Cholesterol, High (4)
  • Cholesteryl Ester Storage Disease & Acid Lipase Deficiency (1)
  • Chondrodysplasia Punctata, Conradi-Hunermann Syndrome (4) *
  • Chondrodysplasia Rhizomelic Dystrophic Punctata (14) *
  • Chorea, Benign Familial (1)
  • Chorea, Syndenham's (7)
  • Choreoathatoid Movements (15)
  • Choreoathatoid, Paroxismal Movement Disorder (1)
  • Chorion Villis Sampling (limb damage from) (2) *
  • Choroid Plexus Papilloma Brain Tumor (3)
  • Chromosome Disorders
  • Chronic Fatigue Syndrome (7) * www.cfids.org
  • Chronic Granulomatous X-Linked Immune Disease (2)
  • Chronic Idiopathic Demyelinating Polyneuropathy (CIDP) (3) *
  • Chronic Lung Disease (29)
  • Chronic Renal Failure (6)
  • Chylothorax (7)*
  • Citrullinemia (Citrulluria) Urea Cycle Disorder (6)*
  • Cleft Cheek (1)
  • Cleft Hand (split hand) (7) *
  • Cleft Laryngo Posterial (2)
  • Cleft Larynx (1)
  • Cleft Lip (115) *www.cleftline.org
  • Cleft Lip and Cleft Palate (104) * www.widesmiles.org/
  • Cleft Lip/Palate pits (Van Der Woude Syndrome) (1)
  • Cleft Lip and Cleft Gums (2)
  • Cleft Nose (3)
  • Cleft Palate (338) *
  • Cleft Palate Submucus (19)*
  • Cleft Staphyloma (1)
  • Cleidocranial Dysostosis (dysplasia) (14) *
  • Cleidocranial Dysplasia (dysostosis) (14) *
  • Clitoroplasty (1)
  • Cloaca Abnormalities (19) **
  • Cloaca Exstrophy (6) *
  • Clostridium Difficile (C-diff) (1)
  • Club Fingers (1) *
  • Club Foot (157) **
  • Club Foot, Bilateral (87) **
  • Club Foot, Unilateral (70)**
  • Club Hand, Radial (3) *
  • Club Wrists (1)*
  • Coarctation of the Aorta (heart defect) (32) *
  • Coats Disease (primary retinal telangectasia) (1)
  • Cobalamin C Deficiency (6) *
  • Cobalamin G Deficiency (2) **
  • Cochlear Hypoplasia (absent cochlear w/common cavity deformity) (1)*
  • Cochlear Implant (8) *
  • Cockayne Syndrome (12) **
  • Coffin-Lowry Syndrome (5) *
  • Coffin-Siris Syndrome (7) **
  • Cohen Syndrome (13) * cohensyndrome@hotmail.com US contact Ellen 662-738-4776
  • Colitis, Ulcerative (4)*
  • Collagen Fibrotic Disease (1)
  • Coloboma (65) *
  • Colostomy (77)
  • Colostomy Reversed (7)
  • Coma (52)
  • Colpocephaly (abnormal enlargement of the occipital horns of the brain) (4)
  • Comatose (40) *
  • Comatose and came out of it (40) *
  • Combined Immune Deficiency Disease (CIDD) (3)
  • Complex I Deficiency, Mitochondrial Myopathy (8) *
  • Complex II: Succinate Dehydrogenase Deficiency (Mitochondrial Disorder) (1)*
  • Complex III Deficiency, Mitochondrial Myopathy (6) *
  • Complex I & II & III Deficiency, Mitochondrial Disorder (1) *
  • Complex I & III Deficiency, Mitochondrial Disorder (1) *
  • Complex I - IV Deficiency, Mitochondrial Disorder (1)*
  • Complex I:NADH dehydrogenase(NADH_CoQ reductase)deficiency (2) *
  • Complex III: Deficiency Mitochondrial Disorder (10)*
  • Complex IV: Cytochrome-C-Oxidase (COX) Deficiency (14) *
  • Complex Cyanotic Congenital Heart (2)
  • Complex Partial Seizures (72)
  • Congenital Adrenal Hyperplasia (21 Hydroxylase Deficiency) (13) **
  • Congenital Chloride Diarrhea (Darrow-Gamble Syndrome) (3) *
  • Conjoined Twins (5)*
  • Conjoined Twins, 1 died (1)*
  • Conjoined Twins, inseparable (1) *
  • Conjoined Twins, joined at abdomen-separated (1) *
  • Conjoined Twins, joined at hips & leg-separated (1) *
  • Conradi-Hunermann Syndrome (9) *
  • Constricted Fiber Bands of the Hand, Congenital (1)
  • Coranalsyntosis (1)
  • Cornea Ulcer (1)
  • Cornelia de Lange Syndrome (26) *
  • Cornelia de Lange Syndrome & Spina Bifida & Arnold-Chiari & RSD (1)
  • Cornelia de Lange Syndrome & Tourette Syndrome (1)
  • Corpus Callosotomy (1)
  • Corpus Callosum, Agenesis of (194) *
  • Cortical Blindness (158) *
  • Cortical Dysplasia (Neuronal Migration Disorder) (4)
  • Costello Syndrome (7) * <
  • Cowden Syndrome (Multiple Hamartoma Syndrome) (4) *
  • Cranio-Fronto-Nasal Dysplasia (3)
  • Craniodiaphyseal Dysplasia, Lenz-Majewski Type (1) *
  • Craniofacial (anomalies of skull or face) (386) * www.ccakids.com/
  • Craniomandibular Dermatodysostis (Mandibuliacral Dysplasia) (1)
  • Craniometaphyseal Dysplasia (1)
  • Craniopharynglioma Brain Tumor (pituitary tumor) (6) *
  • Craniostenosis (2)
  • Craniosynostosis (52) * http://cappskids.org/
  • Craniosynostosis-Arachnodactyly-Hernia (Shpintzen-Goldberg Syndrome) (1)
  • Craniosynostosis of Metopic Sutures (Trigonocephaly) (2)
  • Craniosynostosis, Bi-Lateral Lambdoidal (3)
  • Craniotelencyphalic Dysplasia (1)
  • Craniotomy, Stereotactic Resection (2)
  • Cretinism (iodine deficiency) (1)
  • Cricopharyngeal Achalasia (1)
  • Cri Du Chat Syndrome & Complete Agenesis of the Corpus Callosum (1)
  • Cri Du Chat Syndrome (Cat's Cry) (39) *
  • Crigler Najjar Syndrome Type I (Hyperbilirubinemia) (2)*
  • Crigler Najjar Syndrome Type II (1)*
  • Crohn's Disease (17) *
  • Crouzon Disease (8) ****
  • Crouzon Syndrome & Down Syndrome (1)
  • Cryotherapy (Cryo surgery on eyes) (6)
  • Cryptorchidism (undescended testicles) (86)
  • Cryptothalmos (fused eyelids) (6)
  • Currarino Triad (open or cleft spine) (2) *pw2.netcom.com/~cmperry/currarino.html
  • Cushing Syndrome (1)*
  • Cutaneous, Sacrodosis (skin disorder) (1)
  • Cutaneous, Lichen Amyloidosis (skin disorder) (1)
  • Cutis Laxa (6) * www.orpha.net/nestasso/cutislax
  • Cutis Marmorata Telangiectasia (Van Lohuizen Syndrome) (9) * www.cmtc.nl(Netherlands)
  • Cyclical Vomiting Syndrome (22) **
  • Cystic Adenomotoid Malformation of the Lung (3)
  • Cystic Encephalomalacia (4)
  • Cystic Fibrosis (44) *
  • Cystic Fibrosis & Autism (1)
  • Cystic Fibrosis & Cerebral Palsy (4)
  • Cystic Fibrosis & Duchenne Muscular Dystrophy (1)
  • Cystic Fibrosis & Transposition of Great Vessels (1) *
  • Cystic Hygroma (17) *
  • Cystinosis (4) *
  • Cystinosis+Fanconi Syndrome+Arnold-Chiari Syndrome (1)
  • Cystinosis+Fanconi+Proteinuria+Renal Fanconi's (2)
  • Cystinuria (3) *
  • Cytochrome-C-Oxidase Deficiency (COX Deficiency) (11) *
  • Cytomegalovirus Infection (CMV) (50) *


MUMS: National Parent to Parent Network
Julie J. 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 February 1, 2009 mums@netnet.net