Dandy-Walker malformation
Symptom Information:
Symptom ID: | HPO:0001305 | ||||||||||||||||
Synonyms: |
|
||||||||||||||||
Quality: | |||||||||||||||||
Cross references: |
|
||||||||||||||||
Is a (Direct Parents): |
|
||||||||||||||||
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) |