Dandy-Walker malformation

Symptom Information:

Symptom ID: HPO:0001305
Synonyms:
Dandy-walker anomaly [HPO:0001305]
Dandy-Walker cyst [HPO:0001305]
Dandy Walker malformation [Orphanet:42540]
Dandy-Walker syndrome (disorder) [Orphanet:42540]
Dandy-Walker Syndrome [Orphanet:42540]
Dandy-Walker anomaly [OMIM:Dandy-Walker anomaly]
Dandy-Walker cyst [OMIM:Dandy-Walker cyst]
Dandy-Walker malformation [OMIM:Dandy-Walker malformation]
Dandy-Walker anomaly [Orphanet:42540]
Dandy-Walker syndrome [Orphanet:42540]
Dandy-Walker syndrome [MedDRA:10048411]
Dandy-Walker malformation (1 patient) [OMIM:Dandy-Walker malformation (1 patient)]
Dandy-Walker malformation (WWS) [OMIM:Dandy-Walker malformation (WWS)]
Dandy-Walker malformation (in 1 of 4 patients) [OMIM:Dandy-Walker malformation (in 1 of 4 patients)]
Dandy-Walker malformation (rare) [OMIM:Dandy-Walker malformation (rare)]
Dandy-Walker malformation (variable) [OMIM:Dandy-Walker malformation (variable)]
Quality:
Cross references:
Orphanet:42540 "Dandy-Walker anomaly" [Orphanet:42540]
OMIM: "Dandy-Walker anomaly" [OMIM:Dandy-Walker anomaly]
OMIM: "Dandy-Walker cyst" [OMIM:Dandy-Walker cyst]
OMIM: "Dandy-Walker malformation" [OMIM:Dandy-Walker malformation]
OMIM: "Dandy-Walker malformation (1 patient)" [OMIM:Dandy-Walker malformation (1 patient)]
OMIM: "Dandy-Walker malformation (WWS)" [OMIM:Dandy-Walker malformation (WWS)]
OMIM: "Dandy-Walker malformation (in 1 of 4 patients)" [OMIM:Dandy-Walker malformation (in 1 of 4 patients)]
OMIM: "Dandy-Walker malformation (rare)" [OMIM:Dandy-Walker malformation (rare)]
OMIM: "Dandy-Walker malformation (variable)" [OMIM:Dandy-Walker malformation (variable)]
UMLS:C0010964 "Dandy-Walker Syndrome" [Orphanet:42540]
Is a (Direct Parents):
HPO         Cerebellar vermis hypoplasia
HPO         Widened posterior fossa
MedDRA Cerebral disorders congenital
HPO         Dilated fourth ventricle
HPO         Cerebellar cyst
Orphanet Hydrocephalus
Is a (Whole tree): HPO:
All(HPO:0000001)
    Phenotypic abnormality(HPO:0000118)
       Abnormality of head or neck(HPO:0000152)
          Abnormality of the head(HPO:0000234)
             Abnormality of the skull(HPO:0000929)
                Abnormality of the skull base(HPO:0002693)
                   Abnormality of the posterior cranial fossa(HPO:0000932)
                      Widened posterior fossa(HPO:0005445)
                         Dandy-Walker malformation(HPO:0001305)
       Abnormality of the skeletal system(HPO:0000924)
          Abnormality of skeletal morphology(HPO:0011842)
             Abnormal axial skeleton morphology(HPO:0009121)
                Abnormality of the skull(HPO:0000929)
                   Abnormality of the skull base(HPO:0002693)
                      Abnormality of the posterior cranial fossa(HPO:0000932)
                         Widened posterior fossa(HPO:0005445)
                            Dandy-Walker malformation(HPO:0001305)
MedDRA:
Congenital, familial and genetic disorders(MedDRA:10010331)
    Neurological disorders congenital(MedDRA:10029299)
       Cerebral disorders congenital(MedDRA:10052634)
          Dandy-Walker malformation(HPO:0001305)
Database Frequency: 79 / 7739
Resource:

All diseases associated with this symptom:

3C syndrome (Orphanet:7)
ANTERIOR CHAMBER CLEAVAGE DISORDER, CEREBELLAR HYPOPLASIA, HYPOTHYROIDISM,AND TRACHEAL STENOSIS (OMIM:601427)
Aase-Smith syndrome (Orphanet:916)
Acrocallosal syndrome (Orphanet:36)
Aicardi syndrome (Orphanet:50)
Arthrogryposis with oculomotor limitation and electroretinal anomalies (Orphanet:1154)
Autosomal recessive cutis laxa type 2, classic type (Orphanet:357074)
Autosomal recessive cutis laxa type 2A (Orphanet:357058)
Autosomal recessive deafness-onychodystrophy syndrome (Orphanet:79500)
B4GALT1-CDG (Orphanet:79332)
Beckwith-Wiedemann syndrome (Orphanet:116)
Bohring-Opitz syndrome (Orphanet:97297)
CHARGE syndrome (Orphanet:138)
COFFIN-SIRIS SYNDROME (OMIM:135900)
Cervical hypertrichosis - peripheral neuropathy (Orphanet:2218)
Coffin-Siris syndrome (Orphanet:1465)
Craniosynostosis - Dandy-Walker malformation - hydrocephalus (Orphanet:1538)
DANDY-WALKER MALFORMATION WITH OCCIPITAL CEPHALOCELE, AUTOSOMAL DOMINANT (OMIM:609222)
Dandy-Walker malformation - facial hemangioma (Orphanet:1564)
Dandy-Walker malformation - postaxial polydactyly (Orphanet:1566)
Deafness - onychodystrophy (Orphanet:3231)
Diabetic embryopathy (Orphanet:1926)
Distal monosomy 6p (Orphanet:96125)
EVC2 GENE (OMIM:607261)
Ellis Van Creveld syndrome (Orphanet:289)
Encephalocraniocutaneous lipomatosis (Orphanet:2396)
Facial dysmorphism - macrocephaly - myopia - Dandy-Walker malformation (Orphanet:1970)
Fetal akinesia deformation sequence (Orphanet:994)
Fowler syndrome (Orphanet:221126)
Fryns syndrome (Orphanet:2059)
Galloway-Mowat syndrome (Orphanet:2065)
HYDROLETHALUS SYNDROME 1 (OMIM:236680)
Holoprosencephaly (Orphanet:2162)
Hydrolethalus (Orphanet:2189)
Hypoplasminogenemia (Orphanet:722)
Intellectual deficit, X-linked - Dandy-Walker malformation - basal ganglia disease - Seizures (Orphanet:1568)
Isolated Dandy-Walker malformation (Orphanet:217)
Joubert syndrome 14 (OMIM:614424)
Joubert syndrome 16 (OMIM:614465)
Joubert syndrome 2 (OMIM:608091)
Juberg-Hayward syndrome (Orphanet:2319)
Lethal chondrodysplasia, Moerman type (Orphanet:1420)
Lethal polymalformative syndrome, Boissel type (Orphanet:210144)
Ligneous conjunctivitis (Orphanet:97231)
Linear nevus sebaceus syndrome (Orphanet:2612)
Linear verrucous nevus syndrome (Orphanet:2611)
MENTAL RETARDATION, AUTOSOMAL DOMINANT 16 (OMIM:614609)
MOSAIC VARIEGATED ANEUPLOIDY SYNDROME 1 (OMIM:257300)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 1 (OMIM:236670)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 13 (OMIM:615287)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 5 (OMIM:613153)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 6 (OMIM:613154)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 7 (OMIM:614643)
Macrocephaly - short stature - paraplegia (Orphanet:2427)
Marden-Walker syndrome (Orphanet:2461)
Meckel syndrome (Orphanet:564)
Meckel syndrome, type 1 (OMIM:249000)
Meckel syndrome, type 2 (OMIM:603194)
Meckel syndrome, type 3 (OMIM:607361)
Meckel syndrome, type 4 (OMIM:611134)
Mosaic trisomy 9 (Orphanet:99776)
Mosaic variegated aneuploidy syndrome (Orphanet:1052)
Muscle-eye-brain disease (Orphanet:588)
NPHP3-related Meckel-like syndrome (Orphanet:3032)
Neu-Laxova syndrome (Orphanet:2671)
Neurocutaneous melanocytosis (Orphanet:2481)
Oculocerebral dysplasia (Orphanet:2705)
Oculocerebral hypopigmentation syndrome, Cross type (Orphanet:2719)
Oculocerebrocutaneous syndrome (Orphanet:1647)
Orofaciodigital syndrome type 1 (Orphanet:2750)
PHACE syndrome (Orphanet:42775)
RENAL-HEPATIC-PANCREATIC DYSPLASIA 1 (OMIM:208540)
Renal-genital-middle ear anomalies (Orphanet:1092)
Renal-hepatic-pancreatic dysplasia (Orphanet:294415)
Simpson-Golabi-Behmel syndrome (Orphanet:373)
Smith-Lemli-Opitz syndrome (Orphanet:818)
Toriello-Carey syndrome (Orphanet:3338)
Walker-Warburg syndrome (Orphanet:899)
X-linked dominant chondrodysplasia punctata (Orphanet:35173)