alt.war.civil.usa

"notPythias" wrote in message
news: @ ...
> On 2007-08-14, Flying Fuck < @ > wrote:
>> do you actually think that an albino phenotype can only have albino
>> children?
>
> FF, it's unfortunate that you chose that particular example, because
> you're making good points elsewhere. Unfortunately, albinism is a
> recessive disorder, so albino-phenotype parents really can only have
> albino children.
>
> You are right in general, though. It is entirely possible for
> children
> to have traits that were visible in their parents. When people say
> that
> something has ``skipped a generation,'' that's what they mean.
>
> Both hair and eye color are polygenic (controlled by more than one
> gene), so they cannot be described with simple dominant-recessive
> models, but---
>
> *it is absolutely established that dark-haired people can have blond
> children.*
>
> -nP

And there are unwanted maladies that can be inherited also. I doubt
that these maladies were inherited from the original model but are the
result of mutations.

You say mutations don't occur? Not, for example, according the flu and
HIV viruses.

Some are [Partial List of those beginning with "A"]
Disorder
Mutation
Chromosome

A-T
see ataxia-telangiectasia



AAT
see alpha-1 antitrypsin deficiency



Absence of vas deferens
see congenital bilateral absence of vas deferens



Absent vasa
see congenital bilateral absence of vas deferens



aceruloplasminemia



ACG2
see achondrogenesis type II



ACH
see achondroplasia



Achondrogenesis type II



achondroplasia
substitution


Acid beta-glucosidase deficiency
see Gaucher disease type 1



Acrocephalosyndactyly (Apert)
see Apert syndrome



acrocephalosyndactyly, type V
see Pfeiffer syndrome



Acrocephaly
see Apert syndrome



Acute cerebral Gaucher's disease
see Gaucher disease type 2



acute intermittent porphyria



ACY2 deficiency
see Canavan disease



AD



Adelaide-type craniosynostosis
see Muenke syndrome



Adenomatous Polyposis Coli
see familial adenomatous polyposis



Adenomatous Polyposis of the Colon
see familial adenomatous polyposis



ADP
see ALA dehydratase deficiency



adenylosuccinate lyase deficiency



Adrenal gland disorders
see 21-hydroxylase deficiency



Adrenogenital syndrome
see 21-hydroxylase deficiency



Adrenoleukodystrophy



AIP
see acute intermittent porphyria



AIS
see androgen insensitivity syndrome



AKU
see alkaptonuria



ALA dehydratase porphyria
see ALA dehydratase deficiency



ALA-D porphyria
see ALA dehydratase deficiency



ALA dehydratase deficiency



Alcaptonuria
see alkaptonuria



Alexander disease



alkaptonuria



Alkaptonuric ochronosis
see alkaptonuria



alpha-1 antitrypsin deficiency



alpha-1 proteinase inhibitor
see alpha-1 antitrypsin deficiency



alpha-1 related emphysema
see alpha-1 antitrypsin deficiency



Alpha-galactosidase A deficiency
see Fabry disease
P


ALS
see amyotrophic lateral sclerosis



Alstrom syndrome



ALX
see Alexander disease



Alzheimer disease



Alzheimer's disease
see Alzheimer disease



Amelogenesis Imperfecta
see Amelogenesis imperfecta



Amino levulinic acid dehydratase deficiency
see ALA dehydratase deficiency



Aminoacylase 2 deficiency
see Canavan disease



amyotrophic lateral sclerosis



Anderson-Fabry disease
see Fabry disease
P


androgen insensitivity syndrome



Anemia



Anemia, hereditary sideroblastic
see X-linked sideroblastic anemia

X

Anemia, sex-linked hypochromic sideroblastic
see X-linked sideroblastic anemia

X

Anemia, splenic, familial
see Gaucher disease



Angelman syndrome



Angiokeratoma Corporis Diffusum
see Fabry's disease
P


Angiokeratoma diffuse
see Fabry's disease



Angiomatosis retinae
see von Hippel-Lindau disease



ANH1
see X-linked sideroblastic anemia

X

APC resistance, Leiden type
see factor V Leiden thrombophilia



Apert syndrome



AR deficiency
see androgen insensitivity syndrome



AR-CMT2
see Charcot-Marie-Tooth disease, type 2



Arachnodactyly
see Marfan syndrome



ARNSHL
see Nonsyndromic deafness#autosomal recessive



Arthro-ophthalmopathy, hereditary progressive
see Stickler syndrome#COL2A1



Arthrochalasis multiplex congenita
see Ehlers-Danlos syndrome#arthrochalasia type



AS
see Angelman syndrome



Asp deficiency
see Canavan disease



Aspa deficiency
see Canavan disease



Aspartoacylase deficiency
see Canavan disease



ataxia-telangiectasia



Autism-Dementia-Ataxia-Loss of Purposeful Hand Use syndrome
see Rett syndrome



autosomal dominant juvenile ALS
see amyotrophic lateral sclerosis, type 4



Autosomal dominant opitz G/BBB syndrome
see deletion syndrome
D
22q


See

/wiki/Category:Genetic_disorders

for a longer list.