Partial agenesis of the corpus callosum

Symptom Information:

Symptom ID: HPO:0001338
Synonyms:
Corpus callosum agenesis, partial [HPO:0001338]
Partial agenesis of corpus callosum [HPO:0001338]
Partial corpus callosum agenesis [HPO:0001338]
Partial or complete agenesis of corpus callosum [HPO:0001338]
PARTIAL OR COMPLETE AGENESIS OF THE CORPUS CALLOSUM [HPO:0001338]
Partial to complete agenesis of corpus callosum [HPO:0001338]
Partial-total agenesis of corpus callosum [HPO:0001338]
Corpus callosum agenesis, partial [OMIM:Corpus callosum agenesis, partial]
Partial agenesis of corpus callosum [OMIM:Partial agenesis of corpus callosum]
Partial agenesis of the corpus callosum [OMIM:Partial agenesis of the corpus callosum]
Partial corpus callosum agenesis [OMIM:Partial corpus callosum agenesis]
Partial or complete agenesis of corpus callosum [OMIM:Partial or complete agenesis of corpus callosum]
Partial or complete agenesis of the corpus callosum [OMIM:Partial or complete agenesis of the corpus callosum]
Partial to complete agenesis of corpus callosum [OMIM:Partial to complete agenesis of corpus callosum]
Partial-total agenesis of corpus callosum [OMIM:Partial-total agenesis of corpus callosum]
Partial agenesis of corpus callosum (rare, in males) [OMIM:Partial agenesis of corpus callosum (rare, in males)]
Quality:
Cross references:
OMIM: "Corpus callosum agenesis, partial" [OMIM:Corpus callosum agenesis, partial]
OMIM: "Partial agenesis of corpus callosum" [OMIM:Partial agenesis of corpus callosum]
OMIM: "Partial agenesis of the corpus callosum" [OMIM:Partial agenesis of the corpus callosum]
OMIM: "Partial corpus callosum agenesis" [OMIM:Partial corpus callosum agenesis]
OMIM: "Partial or complete agenesis of corpus callosum" [OMIM:Partial or complete agenesis of corpus callosum]
OMIM: "Partial or complete agenesis of the corpus callosum" [OMIM:Partial or complete agenesis of the corpus callosum]
OMIM: "Partial to complete agenesis of corpus callosum" [OMIM:Partial to complete agenesis of corpus callosum]
OMIM: "Partial-total agenesis of corpus callosum" [OMIM:Partial-total agenesis of corpus callosum]
OMIM: "Partial agenesis of corpus callosum (rare, in males)" [OMIM:Partial agenesis of corpus callosum (rare, in males)]
Is a (Direct Parents):
HPO         Agenesis of corpus callosum
Is a (Whole tree): HPO:
MedDRA:
Database Frequency: 22 / 7739
Resource:

All diseases associated with this symptom:

Aicardi syndrome (Orphanet:50)
Amish lethal microcephaly (Orphanet:99742)
COFFIN-SIRIS SYNDROME (OMIM:135900)
Chudley-McCullough syndrome (Orphanet:314597)
Coffin-Siris syndrome (Orphanet:1465)
Congenital lactic acidosis, Saguenay-Lac-St. Jean type (Orphanet:70472)
Desmosterolosis (Orphanet:35107)
Donnai-Barrow syndrome (Orphanet:2143)
Grubben-de Cock-Borghgraef syndrome (Orphanet:2101)
HOLOPROSENCEPHALY 9 (OMIM:610829)
Intellectual deficit, Buenos-Aires type (Orphanet:3079)
LISSENCEPHALY 6 WITH MICROCEPHALY (OMIM:616212)
Leukoencephalopathy - thalamus and brainstem anomalies - high lactate (Orphanet:314051)
MUSCULAR DYSTROPHY-DYSTROGLYCANOPATHY (CONGENITAL WITH BRAIN AND EYEANOMALIES), TYPE A, 7 (OMIM:614643)
OPITZ-KAVEGGIA SYNDROME (OMIM:305450)
Osteopathia striata - cranial sclerosis (Orphanet:2780)
Pyruvate dehydrogenase E3-binding protein deficiency (Orphanet:255182)
SOTOS SYNDROME 1 (OMIM:117550)
Sotos syndrome (Orphanet:821)
TRICHORRHEXIS NODOSA SYNDROME (OMIM:275550)
TRICHOTHIODYSTROPHY, NONPHOTOSENSITIVE 1 (OMIM:234050)
X-linked complicated corpus callosum dysgenesis (Orphanet:1497)