TDGF1 gene related symptoms and diseases

All the information presented here about the TDGF1 gene and its related diseases, symptoms, and test panels has been aggregated from the following public sources: HGNC,NCBIGENE,ORPHANET, Mendelian Rare Disease Search Engine.

Table of contents:

Rare diseases associated to TDGF1 gene

Here you will find a list of rare diseases related to the TDGF1. You can also use our tool to get a more accurate diagnosis based on your current symptoms.


SEMILOBAR HOLOPROSENCEPHALY

Description

Semilobar holoprosencephaly is one of the classical forms of holoprosencephaly (HPE; see this term) in which the left and right frontal and parietal lobes are fused and the interhemispheric fissure is only present posteriorly.


More info about SEMILOBAR HOLOPROSENCEPHALY

SOURCES: ORPHANET

SEPTOPREOPTIC HOLOPROSENCEPHALY

Alternate names

SEPTOPREOPTIC HOLOPROSENCEPHALY Is also known as septopreoptic hpe

Description

Septopreoptic holoprosencephaly (HPE) is a very rare subtype of lobar HPE (see this term) characterized by midline fusion limited to the septal and/or preoptic regions of the telencephalon without a significant frontal neocortical fusion.


More info about SEPTOPREOPTIC HOLOPROSENCEPHALY

SOURCES: ORPHANET

LOBAR HOLOPROSENCEPHALY

Description

Lobar holoprosencephaly is the mildest classical form of holoprosencephaly (HPE; see this term) characterized by separation of the right and left cerebral hemispheres and lateral ventricules with some continuity across the frontal neocortex, especially rostrally and ventrally.


More info about LOBAR HOLOPROSENCEPHALY

SOURCES: ORPHANET

ALOBAR HOLOPROSENCEPHALY

Description

Alobar holoprosencephaly is the most severe classical form of holoprosencephaly (HPE; see this term) characterized by a single brain ventricle and no interhemispheric fissure.


More info about ALOBAR HOLOPROSENCEPHALY

SOURCES: ORPHANET

MIDLINE INTERHEMISPHERIC VARIANT OF HOLOPROSENCEPHALY

Alternate names

MIDLINE INTERHEMISPHERIC VARIANT OF HOLOPROSENCEPHALY Is also known as mihf, mihv, middle interhemispheric variant of holoprosencephaly, mih, mih type hpe, syntelencephaly, middle interhemispheric fusion variant

Description

Midline interhemispheric variant of holoprosencephaly (MIH) or syntelencephaly is a form of holoprosencephaly (HPE; see this term) characterized by non-separation of the posterior frontal and parietal lobes, normally-formed callosal genu and splenium, absence of the callosal body, normally-separated hypothalamus and lentiform nucleus, and frequent heterotopic gray matter.


More info about MIDLINE INTERHEMISPHERIC VARIANT OF HOLOPROSENCEPHALY

SOURCES: ORPHANET



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